Canonical Allele Identifier: PA2825579713
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6548

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108450.1:p.Arg337Gly
CA340600
NM_001114978.2:c.1009C>G