Canonical Allele Identifier: PA2826567441
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376596
ClinVar RCV Id: RCV000418371 RCV000417655 RCV000417883 RCV000425994 RCV000427865 RCV000430718 RCV000436003 RCV000436185 RCV000438999 RCV000785257 RCV001362325 RCV002418243
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Phe231Ile
CA16603018
NM_001276761.3:c.691T>A