Allele Registry

Canonical Allele Identifier: PA2825650396

Gene: GSN HGNC NCBI

ClinVar RCV:

RCV000017564

RCV000489240

RCV002362587

ClinVar Variation:

16180

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121135.2:p.Asp199Asn	CA250652 NM_001127663.2:c.595G>A