Canonical Allele Identifier: PA111708
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6533
ClinVar RCV Id: RCV000006907 RCV000006906 RCV000478736 RCV000548176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003713.3:p.Arg318His
CA118339
NM_003722.5:c.953G>A