Allele Registry

Canonical Allele Identifier: PA2826401537

Gene: CHRND HGNC NCBI

ClinVar Allele:

360838

ClinVar RCV:

RCV000414846

ClinVar Variation:

374185

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243586.1:p.Trp447Leu	CA16043388 NM_001256657.2:c.1340G>T