Canonical Allele Identifier: PA2827264761
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6548

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316075.1:p.Arg158Gly
CA340600
NM_001329146.2:c.472C>G