Canonical Allele Identifier: PA114615
Gene: CISD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 892
ClinVar RCV Id: RCV000000940
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008389.1:p.Glu37Gln
CA114614
NM_001008388.5:c.109G>C