Canonical Allele Identifier: PA101227
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_000168.1:p.Asp214Tyr
CA250654
NM_000177.5:c.640G>T