Canonical Allele Identifier: PA2827570286
Gene: NALCN HGNC NCBI

Linked Data

ClinVar Variation Id: 88687
ClinVar RCV Id: RCV000074370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337680.1:p.Trp1258Leu
CA145297
NM_001350751.2:c.3773G>T