Canonical Allele Identifier: PA2579936591
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1460570
ClinVar RCV Id: RCV001951660

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Thr123Ser
CA397844287
NM_000546.6:c.368C>G
CA397844300
NM_000546.6:c.367A>T