Allele Registry

Canonical Allele Identifier: PA2826451865

Gene: GSN HGNC NCBI

ClinVar RCV:

RCV000017565

RCV003556034

ClinVar Variation:

16181

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244958.1:p.Asp180Tyr	CA250654 NM_001258029.2:c.538G>T