Canonical Allele Identifier: PA915989131
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 706220
ClinVar RCV Id: RCV000876757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005129.2:p.Glu152Asp
CA10321202
NM_005138.3:c.456A>T
CA412192666
NM_005138.3:c.456A>C