Canonical Allele Identifier: PA2580282039
Gene: SCG2 HGNC NCBI
ClinVar RCV:
RCV004202417
ClinVar Variation:
2366049
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Amino-acid Alleles

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