Canonical Allele Identifier: PA2573243790
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1353618
ClinVar RCV Id: RCV001863506 RCV002478111
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005129.2:p.Arg206Cys
CA10321158
NM_005138.3:c.616C>T