Canonical Allele Identifier: PA2827700980
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_001339997.1:p.Asp174Tyr
CA250654
NM_001353068.2:c.520G>T