Allele Registry

Canonical Allele Identifier: PA169229

Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142714

ClinVar RCV Id: RCV000132084 RCV000420354 RCV000422710 RCV000433401 RCV000435205 RCV000440576 RCV000432346 RCV000441079 RCV000417987 RCV000423376 RCV000428641 RCV000441725 RCV000464261 RCV000431054 RCV000581940 RCV000785336 RCV001271055 RCV001527088 RCV001567943 RCV003462031

ClinVar Variation Id: 634770

ClinVar RCV Id: RCV000785508 RCV002370058 RCV003332249 RCV003472321 RCV003509608

ClinVar Variation Id: 1757269

ClinVar RCV Id: RCV002367440 RCV004055277

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119588.1:p.Met105Ile	CA000349 NM_001126116.1:c.315G>A CA287488024 NM_001126116.1:c.315G>T CA287488027 NM_001126116.1:c.315G>C