Allele Registry

Canonical Allele Identifier: PA2826942577

Gene: CHRND HGNC NCBI

ClinVar Allele:

191169

ClinVar RCV:

RCV000174260

RCV000530315

RCV001142919

RCV001657944

RCV003891709

ClinVar Variation:

194006

HGVS (amino-acid)	Matching Registered Transcripts
NP_001298125.1:p.Arg366His	CA200909 NM_001311196.2:c.1097G>A