Canonical Allele Identifier: PA338069
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 216469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Tyr104His
CA338059
NM_001126117.1:c.310T>C