Canonical Allele Identifier: PA2827569979
Gene: NALCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1804284
ClinVar RCV Id: RCV002469585
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337680.1:p.Ser338Leu
CA7036345
NM_001350751.2:c.1013C>T