Canonical Allele Identifier: PA2826565578
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1019369
ClinVar RCV Id: RCV001318797

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Thr172Ser
CA397840130
NM_001276760.3:c.515C>G
CA397840132
NM_001276760.3:c.514A>T