Canonical Allele Identifier: PA2579934322
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376678
ClinVar RCV Id: RCV000418040 RCV000420871 RCV000422877 RCV000422166 RCV000428087 RCV000428696 RCV000429377 RCV000433566 RCV000435261 RCV000440106 RCV000439367 RCV000701251
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Val274Leu
CA16603092
NM_000546.6:c.820G>C