Allele Registry

SUSPENSION NOTICE:2024-08-07T19:00:00-0500 — 2024-09-25T08:00:00-0500
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Canonical Allele Identifier: PA2826401504

Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 2181412

ClinVar RCV Id: RCV002606134 RCV003143501

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243586.1:p.Phe386Leu	CA2168287 NM_001256657.2:c.1158C>G CA351005241 NM_001256657.2:c.1156T>C CA351005246 NM_001256657.2:c.1158C>A