Canonical Allele Identifier: PA1139719736
Gene: FIG4 HGNC NCBI

Linked Data

ClinVar Variation Id: 859627
ClinVar RCV Id: RCV001065785
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055660.1:p.Ile41Val
CA365211369
NM_014845.6:c.121A>G