Canonical Allele Identifier: PA2827569977
Gene: NALCN HGNC NCBI

Linked Data

ClinVar Variation Id: 985383
ClinVar RCV Id: RCV001266253
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337680.1:p.Arg329Thr
CA388704761
NM_001350751.2:c.986G>C