Canonical Allele Identifier: PA2828167191
Gene: NBEAL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 345661
ClinVar RCV Id: RCV000322227
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352045.1:p.Ser1356Leu
CA2361159
NM_001365116.2:c.4067C>T