Allele Registry

Canonical Allele Identifier: PA2826942318

Gene: CHRND HGNC NCBI

ClinVar Allele:

360838

ClinVar RCV:

RCV000414846

ClinVar Variation:

374185

HGVS (amino-acid)	Matching Registered Transcripts
NP_001298124.1:p.Trp268Leu	CA16043388 NM_001311195.2:c.803G>T