Canonical Allele Identifier: PA2827568535
Gene: NALCN HGNC NCBI

Linked Data

ClinVar Variation Id: 235834
ClinVar RCV Id: RCV000224900

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337677.1:p.Thr513Asn
CA10581445
NM_001350748.2:c.1538C>A