Canonical Allele Identifier: PA095841
Gene: FIG4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1728

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055660.1:p.Asp53Tyr
CA251934
NM_014845.6:c.157G>T