Canonical Allele Identifier: PA2826401508
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 286380
ClinVar RCV Id: RCV000360639 RCV000764382 RCV001855172
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243586.1:p.Arg392Gln
CA2168293
NM_001256657.2:c.1175G>A