Canonical Allele Identifier: PA916026958
Gene: SVIL HGNC NCBI

Linked Data

ClinVar Variation Id: 402169
ClinVar RCV Id: RCV000454313
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310528.1:p.Ser899Leu
CA5456867
NM_001323599.2:c.2696C>T