Canonical Allele Identifier: PA2826942545
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_001298125.1:p.Arg306Gln
CA2168293
NM_001311196.2:c.917G>A