Canonical Allele Identifier: PA2825580686
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108453.1:p.Asp257Gly
CA118341
NM_001114981.1:c.770A>G