Canonical Allele Identifier: PA2827265131
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6527

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316077.1:p.Arg243Trp
CA118334
NM_001329148.2:c.727C>T