Canonical Allele Identifier: PA2827265562
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316078.1:p.Asp257Gly
CA118341
NM_001329149.2:c.770A>G