Canonical Allele Identifier: PA2579935372
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1019369
ClinVar RCV Id: RCV001318797

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Thr211Ser
CA397840130
NM_000546.6:c.632C>G
CA397840132
NM_000546.6:c.631A>T