Canonical Allele Identifier: PA2580282039
Gene: SCG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2366049
ClinVar RCV Id: RCV004202417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003460.2:p.Gln557Leu
CA2137936
NM_003469.5:c.1670A>T