Canonical Allele Identifier: PA2826059072
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3063990
ClinVar RCV Id: RCV003988578
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162580.1:p.Ala97Ser
CA10321242
NM_001169109.2:c.289G>T