Canonical Allele Identifier: PA2827281531
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 1716376
ClinVar RCV Id: RCV002304670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316893.1:p.Cys242Arg
CA355753740
NM_001329964.2:c.724T>C