Canonical Allele Identifier: PA169587
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142854

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Pro33Ala
CA000070
NM_001126118.1:c.97C>G