Canonical Allele Identifier: PA2827265145
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6550

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316077.1:p.Arg266Gln
CA118348
NM_001329148.2:c.797G>A