Allele Registry

Canonical Allele Identifier: PA2827568903

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000416437

ClinVar Variation:

375369

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337678.1:p.Met547Val	CA16044231 NM_001350749.2:c.1639A>G