Canonical Allele Identifier: PA645442284
Gene: NBEAL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 345673
ClinVar RCV Id: RCV000266343 RCV003950214
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055990.1:p.Thr1786Ser
CA2361524
NM_015175.3:c.5356A>T