Canonical Allele Identifier: PA111747
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6540

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003713.3:p.Arg337Gln
CA340599
NM_003722.5:c.1010G>A