Allele Registry

Canonical Allele Identifier: PA2826401417

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV000020032

ClinVar Variation:

18364

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243586.1:p.Pro256Gln	CA128063 NM_001256657.2:c.767C>A