Canonical Allele Identifier: PA2826059532
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 139088
ClinVar RCV Id: RCV000284953 RCV000369274 RCV000431453 RCV000383650 RCV001145436
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162581.1:p.Ala259Val
CA293456
NM_001169110.1:c.776C>T