Allele Registry

Canonical Allele Identifier: PA238634

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV000173168

RCV000557059

RCV000724009

ClinVar Variation:

193123

HGVS (amino-acid)	Matching Registered Transcripts
NP_000742.1:p.Ala15Val	CA238633 NM_000751.2:c.44C>T