Canonical Allele Identifier: PA250655
Gene: GSN HGNC NCBI

Linked Data

ClinVar Variation Id: 16181
ClinVar RCV Id: RCV000017565 RCV003556034
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121138.1:p.Asp174Tyr
CA250654
NM_001127666.2:c.520G>T