Canonical Allele Identifier: PA2825579723
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 208418
ClinVar RCV Id: RCV000190455
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108450.1:p.Ala346Gly
CA204448
NM_001114978.2:c.1037C>G