Canonical Allele Identifier: PA095888
Gene: FIG4 HGNC NCBI

Linked Data

ClinVar Variation Id: 50996

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055660.1:p.Leu175Pro
CA143925
NM_014845.6:c.524T>C