Allele Registry

Canonical Allele Identifier: PA645443946

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV000485087

RCV000805114

RCV001332575

ClinVar Variation:

420109

HGVS (amino-acid)	Matching Registered Transcripts
NP_000742.1:p.Arg43Trp	CA2167903 NM_000751.2:c.127C>T