Canonical Allele Identifier: PA095902
Gene: FIG4 HGNC NCBI

Linked Data

ClinVar Variation Id: 156014
ClinVar RCV Id: RCV000144071 RCV000697297 RCV003447113
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055660.1:p.Leu17Pro
CA270671
NM_014845.6:c.50T>C