Canonical Allele Identifier: PA658809821
Gene: FIG4 HGNC NCBI

Linked Data

ClinVar Variation Id: 543322

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055660.1:p.Gln195Leu
CA3955841
NM_014845.6:c.584A>T