Canonical Allele Identifier: PA2579953818
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 572378

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Pro71Ser
CA397845838
NM_000546.6:c.211C>T