Allele Registry

Canonical Allele Identifier: PA2826451864

Gene: GSN HGNC NCBI

ClinVar RCV:

RCV000017564

RCV000489240

RCV002362587

ClinVar Variation:

16180

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244958.1:p.Asp180Asn	CA250652 NM_001258029.2:c.538G>A