Canonical Allele Identifier: PA2825579722
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6529
ClinVar RCV Id: RCV000006902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108450.1:p.Cys345Arg
CA118336
NM_001114978.2:c.1033T>C