Canonical Allele Identifier: PA2827704639
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_001340005.1:p.Asp187Tyr
CA250654
NM_001353076.2:c.559G>T