Canonical Allele Identifier: PA916027719
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6528
ClinVar RCV Id: RCV000006901 RCV000705452 RCV001804714 RCV002250454
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316079.1:p.Arg64Gln
CA118335
NM_001329150.2:c.191G>A