Canonical Allele Identifier: PA2826059701
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1315170
ClinVar RCV Id: RCV001773364
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162582.1:p.Gln146_Val148del
CA640357305
NM_001169111.2:c.437_445del