Allele Registry

Canonical Allele Identifier: PA2825650397

Gene: GSN HGNC NCBI

ClinVar RCV:

RCV000017565

RCV003556034

ClinVar Variation:

16181

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121135.2:p.Asp199Tyr	CA250654 NM_001127663.2:c.595G>T