Canonical Allele Identifier: PA2580282024
Gene: SCG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2313927
ClinVar RCV Id: RCV004160876
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003460.2:p.Gln31His
CA351128635
NM_003469.5:c.93G>C
CA351128636
NM_003469.5:c.93G>T