Allele Registry

Canonical Allele Identifier: PA2826452316

Gene: GSN HGNC NCBI

ClinVar RCV:

RCV000017565

RCV003556034

ClinVar Variation:

16181

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244959.1:p.Asp171Tyr	CA250654 NM_001258030.2:c.511G>T