Canonical Allele Identifier: PA2827569973
Gene: NALCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1809774
ClinVar RCV Id: RCV002505989
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337680.1:p.Ile322Met
CA388704806
NM_001350751.2:c.966T>G