Allele Registry

Canonical Allele Identifier: PA2826452315

Gene: GSN HGNC NCBI

ClinVar RCV:

RCV000017564

RCV000489240

RCV002362587

ClinVar Variation:

16180

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244959.1:p.Asp171Asn	CA250652 NM_001258030.2:c.511G>A