Canonical Allele Identifier: PA2826564088
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1019369
ClinVar RCV Id: RCV001318797

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Thr52Ser
CA397840130
NM_001276699.3:c.155C>G
CA397840132
NM_001276699.3:c.154A>T