Canonical Allele Identifier: PA2826567577
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406594
ClinVar RCV Id: RCV000471030
ClinVar Variation Id: 1061526
ClinVar RCV Id: RCV001371121

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Lys252Gln
CA16615698
NM_001276761.3:c.753_754delinsAC
CA397836584
NM_001276761.3:c.754A>C