Allele Registry

Canonical Allele Identifier: PA110470

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV000020034

ClinVar Variation:

18366

HGVS (amino-acid)	Matching Registered Transcripts
NP_000742.1:p.Glu80Lys	CA128066 NM_000751.2:c.238G>A