Canonical Allele Identifier: PA2827281537
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 208163

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316893.1:p.His245Arg
CA339766
NM_001329964.2:c.734A>G