Canonical Allele Identifier: PA2825579731
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108450.1:p.Asp351Gly
CA118341
NM_001114978.2:c.1052A>G