Canonical Allele Identifier: PA2827695500
Gene: GSN HGNC NCBI

Linked Data

ClinVar Variation Id: 16181
ClinVar RCV Id: RCV000017565 RCV003556034
JSON-LD

Amino-acid Alleles

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