Canonical Allele Identifier: PA2828167180
Gene: NBEAL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1684436
ClinVar RCV Id: RCV002245442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352045.1:p.Arg1328Gln
CA2361140
NM_001365116.2:c.3983G>A