Canonical Allele Identifier: PA645442311
Gene: NBEAL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 345683
ClinVar RCV Id: RCV000281014 RCV000893189 RCV001270527 RCV001821049 RCV003910360
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055990.1:p.Arg2289Gln
CA2361979
NM_015175.3:c.6866G>A