Allele Registry

Canonical Allele Identifier: PA2827568478

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000416463

RCV001092912

RCV002521493

ClinVar Variation:

375370

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337677.1:p.Ile322Thr	CA16044232 NM_001350748.2:c.965T>C