Canonical Allele Identifier: PA2829805560
Gene: NBEAL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3179142
ClinVar RCV Id: RCV004467496
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055990.1:p.Pro1386Ser
CA2361153
NM_015175.3:c.4156C>T