Canonical Allele Identifier: PA2825579702
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6532
ClinVar RCV Id: RCV000006905 RCV001280776 RCV002512857 RCV003162215
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108450.1:p.Arg319Cys
CA118338
NM_001114978.2:c.955C>T