Canonical Allele Identifier: PA2827570040
Gene: NALCN HGNC NCBI

Linked Data

ClinVar Variation Id: 420820
ClinVar RCV Id: RCV000483143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337680.1:p.Asp529Gly
CA16619609
NM_001350751.2:c.1586A>G