Canonical Allele Identifier: PA2580282037
Gene: SCG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2384241
ClinVar RCV Id: RCV004222000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003460.2:p.Arg490Ser
CA351122785
NM_003469.5:c.1470A>T
CA351122786
NM_003469.5:c.1470A>C