Allele Registry

Canonical Allele Identifier: PA2827569469

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000416437

ClinVar Variation:

375369

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337679.1:p.Met518Val	CA16044231 NM_001350750.2:c.1552A>G