Canonical Allele Identifier: PA2741899850
Gene: SCG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2596822
ClinVar RCV Id: RCV004336101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003460.2:p.Ile311Asn
CA66460635
NM_003469.5:c.932T>A