Canonical Allele Identifier: PA2827568554
Gene: NALCN HGNC NCBI

Linked Data

ClinVar Variation Id: 420820
ClinVar RCV Id: RCV000483143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337677.1:p.Asp558Gly
CA16619609
NM_001350748.2:c.1673A>G