Canonical Allele Identifier: PA2826059520
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1374485
ClinVar RCV Id: RCV001883113
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162581.1:p.Asp252Glu
CA10321116
NM_001169110.1:c.756C>G
CA412190367
NM_001169110.1:c.756C>A