Allele Registry

Canonical Allele Identifier: PA250655

Gene: GSN HGNC NCBI

ClinVar RCV:

RCV000017565

RCV003556034

ClinVar Variation:

16181

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121138.1:p.Asp174Tyr	CA250654 NM_001127666.2:c.520G>T