Canonical Allele Identifier: PA2580327012
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2122637
ClinVar RCV Id: RCV003054149
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005129.2:p.Gly72Asp
CA412193597
NM_005138.3:c.215G>A