Allele Registry

Canonical Allele Identifier: PA101214

Gene: GSN HGNC NCBI

ClinVar RCV:

RCV000017564

RCV000489240

RCV002362587

ClinVar Variation:

16180

HGVS (amino-acid)	Matching Registered Transcripts
NP_000168.1:p.Asp214Asn	CA250652 NM_000177.5:c.640G>A