Allele Registry

Canonical Allele Identifier: PA101227

Gene: GSN HGNC NCBI

ClinVar RCV:

RCV000017565

RCV003556034

ClinVar Variation:

16181

HGVS (amino-acid)	Matching Registered Transcripts
NP_000168.1:p.Asp214Tyr	CA250654 NM_000177.5:c.640G>T