Allele Registry

Canonical Allele Identifier: PA2826942569

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV000542114

RCV000762329

RCV001141061

ClinVar Variation:

466190

HGVS (amino-acid)	Matching Registered Transcripts
NP_001298125.1:p.Asn355Ser	CA2168330 NM_001311196.2:c.1064A>G