Allele Registry

Canonical Allele Identifier: PA2826942566

Gene: CHRND HGNC NCBI

ClinVar Variation Id: 953201

HGVS (amino-acid)	Matching Registered Transcripts
NP_001298125.1:p.Ile344Thr	CA2168324 NM_001311196.2:c.1031T>C