Allele Registry

Canonical Allele Identifier: PA2826942217

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV000289236

RCV000724895

RCV000764381

RCV001081973

RCV003140299

ClinVar Variation:

281423

2431232

HGVS (amino-acid)	Matching Registered Transcripts
NP_001298124.1:p.Pro113Ser	CA2168190 NM_001311195.2:c.337C>T CA2580066055 NM_001311195.2:c.337_338delinsAG