Allele Registry

Canonical Allele Identifier: PA095850

Gene: FIG4 HGNC NCBI

ClinVar RCV:

RCV000144074

RCV003447115

ClinVar Variation:

156017

HGVS (amino-acid)	Matching Registered Transcripts
NP_055660.1:p.Asp783Val	CA170743 NM_014845.6:c.2348A>T