Canonical Allele Identifier: PA2827281751
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6545
ClinVar RCV Id: RCV000006920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316893.1:p.Ser578Pro
CA118343
NM_001329964.2:c.1732T>C