Canonical Allele Identifier: PA2827570021
Gene: NALCN HGNC NCBI

Linked Data

ClinVar Variation Id: 235834
ClinVar RCV Id: RCV000224900

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337680.1:p.Thr484Asn
CA10581445
NM_001350751.2:c.1451C>A