Allele Registry

Canonical Allele Identifier: PA2827569162

Gene: NALCN HGNC NCBI

ClinVar Allele:

94267

ClinVar RCV:

RCV000074370

ClinVar Variation:

88687

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337678.1:p.Trp1287Leu	CA145297 NM_001350749.2:c.3860G>T