Canonical Allele Identifier: PA2826059045
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1962506
ClinVar RCV Id: RCV002726183
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162580.1:p.Trp75Gly
CA412193563
NM_001169109.2:c.223T>G
CA2580099987
NM_001169109.2:c.222_223delinsGG