Canonical Allele Identifier: PA2827281511
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 730540
ClinVar RCV Id: RCV001513730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316893.1:p.Ile223Val
CA2752223
NM_001329964.2:c.667A>G