Canonical Allele Identifier: PA2827569116
Gene: NALCN HGNC NCBI

Linked Data

ClinVar Variation Id: 235831
ClinVar RCV Id: RCV000224193
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337678.1:p.Thr1165Pro
CA10581442
NM_001350749.2:c.3493A>C