Canonical Allele Identifier: PA915989132
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 5680
ClinVar RCV Id: RCV000006034 RCV001851687
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005129.2:p.Arg171Trp
CA117676
NM_005138.3:c.511C>T