Allele Registry

Canonical Allele Identifier: PA2827699147

Gene: GSN HGNC NCBI

ClinVar RCV:

RCV000017565

RCV003556034

ClinVar Variation:

16181

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339993.1:p.Asp174Tyr	CA250654 NM_001353064.2:c.520G>T