Canonical Allele Identifier: PA2826401517
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 2418687
ClinVar RCV Id: RCV003121436
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243586.1:p.Arg398Leu
CA351005321
NM_001256657.2:c.1193G>T