Canonical Allele Identifier: PA2828167207
Gene: NBEAL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 345662
ClinVar RCV Id: RCV000379070

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352045.1:p.Gly1382Ser
CA2361181
NM_001365116.2:c.4144G>A