Canonical Allele Identifier: PA916006485
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 43588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Pro8Ser
CA000053
NM_001276761.3:c.22C>T