Canonical Allele Identifier: PA916030628
Gene: NALCN HGNC NCBI
ClinVar Allele:
94267
ClinVar RCV:
RCV000074370
ClinVar Variation:
88687
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337677.1:p.Trp1316Leu
CA145297
NM_001350748.2:c.3947G>T