Canonical Allele Identifier: PA122169
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12353
ClinVar RCV Id: RCV000013147 RCV000566103 RCV000794324 RCV000785500 RCV001823095 RCV003128570
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Val25Phe
CA000222
NM_001126116.1:c.73G>T