Canonical Allele Identifier: PA2579935783
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376017
ClinVar RCV Id: RCV000420735 RCV000421990 RCV000419648 RCV000420982 RCV000428561 RCV000430804 RCV000437348 RCV000432237 RCV000438619 RCV000438785 RCV000439921 RCV000437553 RCV000426247 RCV000445170 RCV000430991 RCV000436282 RCV000775880 RCV001237773 RCV002289516
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Val173Ala
CA16602486
NM_000546.6:c.518T>C