Allele Registry

Canonical Allele Identifier: PA2827695500

Gene: GSN HGNC NCBI

ClinVar RCV:

RCV000017565

RCV003556034

ClinVar Variation:

16181

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339985.1:p.Asp163Tyr	CA250654 NM_001353056.2:c.487G>T