Canonical Allele Identifier: PA2499270149
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_005129.2:p.Gln101His
CA10321239
NM_005138.3:c.303G>C
CA412193158
NM_005138.3:c.303G>T