Canonical Allele Identifier: PA111764
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 279913
ClinVar RCV Id: RCV000371222 RCV001050126 RCV003152702
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003713.3:p.Arg343Trp
CA10602901
NM_003722.5:c.1027C>T