Canonical Allele Identifier: PA2828166904
Gene: NBEAL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 345632
ClinVar RCV Id: RCV000305249 RCV000595231 RCV001821044
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352045.1:p.Gly616Arg
CA2360502
NM_001365116.2:c.1846G>A
CA352508985
NM_001365116.2:c.1846G>C