Allele Registry

Canonical Allele Identifier: PA2826942472

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV000289236

RCV000724895

RCV000764381

RCV001081973

RCV003140299

ClinVar Variation:

281423

2431232

HGVS (amino-acid)	Matching Registered Transcripts
NP_001298125.1:p.Pro206Ser	CA2168190 NM_001311196.2:c.616C>T CA2580066055 NM_001311196.2:c.616_617delinsAG