Allele Registry

Canonical Allele Identifier: PA1139680212

Gene: CHRND HGNC NCBI

ClinVar Variation Id: 953201

HGVS (amino-acid)	Matching Registered Transcripts
NP_000742.1:p.Ile445Thr	CA2168324 NM_000751.2:c.1334T>C