Canonical Allele Identifier: PA2573223368
Gene: GNS HGNC NCBI

Linked Data

ClinVar Variation Id: 1519948
ClinVar RCV Id: RCV002024852
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002067.1:p.Thr389Ile
CA238279746
NM_002076.4:c.1166C>T