Canonical Allele Identifier: PA2825580889
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 903493
ClinVar RCV Id: RCV001150860 RCV001150861 RCV001150859 RCV001354747
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108454.1:p.Val136Leu
CA2752227
NM_001114982.2:c.406G>C