Canonical Allele Identifier: PA2827281591
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6548

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316893.1:p.Arg335Gly
CA340600
NM_001329964.2:c.1003C>G