Canonical Allele Identifier: PA2827281541
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6550

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316893.1:p.Arg264Gln
CA118348
NM_001329964.2:c.791G>A