Canonical Allele Identifier: PA2826059659
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1054726
ClinVar RCV Id: RCV001363284
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162582.1:p.Gln101His
CA10321239
NM_001169111.2:c.303G>C
CA412193158
NM_001169111.2:c.303G>T