Canonical Allele Identifier: PA2573172722
Gene: SI HGNC NCBI

Linked Data

ClinVar Variation Id: 1553819
ClinVar RCV Id: RCV002180622 RCV003355798
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001032.2:p.Thr122Ala
CA2691538
NM_001041.4:c.364A>G