Allele Registry

Canonical Allele Identifier: PA2826942441

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV000538556

RCV001357055

ClinVar Variation:

466196

HGVS (amino-acid)	Matching Registered Transcripts
NP_001298125.1:p.Arg142His	CA2168126 NM_001311196.2:c.425G>A