Canonical Allele Identifier: PA645468611
Gene: FIG4 HGNC NCBI

Linked Data

ClinVar Variation Id: 355037
ClinVar RCV Id: RCV000288549 RCV000343538 RCV001095019 RCV001545776
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055660.1:p.Ala117Val
CA3955749
NM_014845.6:c.350C>T