Canonical Allele Identifier: PA2826566534
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 572378

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Pro32Ser
CA397845838
NM_001276761.3:c.94C>T