Canonical Allele Identifier: PA2829460004
Gene: SCG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3158387
ClinVar RCV Id: RCV004452777
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003460.2:p.Ile352Val
CA2138034
NM_003469.5:c.1054A>G