Canonical Allele Identifier: PA336904
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 216473
ClinVar RCV Id: RCV000197011
ClinVar Variation Id: 1047514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Gly170Arg
CA336894
NM_001126117.1:c.508G>C
CA397836336
NM_001126117.1:c.508G>A