Canonical Allele Identifier: PA2827264555
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6548

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316074.1:p.Arg243Gly
CA340600
NM_001329145.2:c.727C>G