Allele Registry

Canonical Allele Identifier: PA2827695047

Gene: GSN HGNC NCBI

ClinVar RCV:

RCV000017564

RCV000489240

RCV002362587

ClinVar Variation:

16180

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339984.1:p.Asp163Asn	CA250652 NM_001353055.2:c.487G>A