Canonical Allele Identifier: PA2580134551
Gene: SI HGNC NCBI

Linked Data

ClinVar Variation Id: 1950381
ClinVar RCV Id: RCV002671749
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001032.2:p.Val116Phe
CA355035361
NM_001041.4:c.346G>T