Canonical Allele Identifier: PA2827569122
Gene: NALCN HGNC NCBI

Linked Data

ClinVar Variation Id: 188046
ClinVar RCV Id: RCV000167764 RCV000224736 RCV001267339 RCV001390781
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337678.1:p.Arg1181Gln
CA212642
NM_001350749.2:c.3542G>A