Canonical Allele Identifier: PA2741914403
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_005129.2:p.Ala97Ser
CA10321242
NM_005138.3:c.289G>T