ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827705095
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_001340006.1:p.Asp174Tyr
CA250654
NM_001353077.1:c.520G>T