Canonical Allele Identifier: PA916006288
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376574
ClinVar RCV Id: RCV000418555 RCV000417498 RCV000422481 RCV000422719 RCV000425072 RCV000427235 RCV000427531 RCV000428817 RCV000433989 RCV000432745 RCV000435343 RCV000433862 RCV000435149 RCV000439349 RCV000440369 RCV000442469 RCV000444988 RCV000473420 RCV002365459 RCV004022207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Cys79Phe
CA16603000
NM_001276699.3:c.236G>T