Allele Registry

Canonical Allele Identifier: PA645444195

Gene: CHRND HGNC NCBI

ClinVar Allele:

360838

ClinVar RCV:

RCV000414846

ClinVar Variation:

374185

HGVS (amino-acid)	Matching Registered Transcripts
NP_000742.1:p.Trp462Leu	CA16043388 NM_000751.2:c.1385G>T