Canonical Allele Identifier: PA2826401418
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 256781
ClinVar RCV Id: RCV000551038 RCV001711662 RCV003891859
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243586.1:p.Asp258Asn
CA2168139
NM_001256657.2:c.772G>A