Canonical Allele Identifier: PA111682
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6550
ClinVar RCV Id: RCV000006926 RCV000006925 RCV000413620 RCV001390108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003713.3:p.Arg266Gln
CA118348
NM_003722.5:c.797G>A