Canonical Allele Identifier: PA658800983
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 534531
ClinVar RCV Id: RCV000642116
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000742.1:p.Arg413Ser
CA351005319
NM_000751.2:c.1237C>A