Canonical Allele Identifier: PA2827281738
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 689635
ClinVar RCV Id: RCV000850386
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316893.1:p.Leu560Pro
CA355758994
NM_001329964.2:c.1679T>C