Allele Registry

Canonical Allele Identifier: PA110485

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV000020032

ClinVar Variation:

18364

HGVS (amino-acid)	Matching Registered Transcripts
NP_000742.1:p.Pro271Gln	CA128063 NM_000751.2:c.812C>A