Canonical Allele Identifier: PA916027724
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6550

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316079.1:p.Arg87Gln
CA118348
NM_001329150.2:c.260G>A