Allele Registry

Canonical Allele Identifier: PA2826942453

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV000020032

ClinVar Variation:

18364

HGVS (amino-acid)	Matching Registered Transcripts
NP_001298125.1:p.Pro170Gln	CA128063 NM_001311196.2:c.509C>A