Canonical Allele Identifier: PA2827281610
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316893.1:p.Asp349Gly
CA118341
NM_001329964.2:c.1046A>G