Canonical Allele Identifier: PA2828167158
Gene: NBEAL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2572162
ClinVar RCV Id: RCV003313900

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352045.1:p.Pro1269Thr
CA2361105
NM_001365116.2:c.3805C>A