Canonical Allele Identifier: PA2827265127
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 1392776
ClinVar RCV Id: RCV001912395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316077.1:p.Val237Ile
CA2752230
NM_001329148.2:c.709G>A