Canonical Allele Identifier: PA096182
Gene: SCN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 60770
ClinVar RCV Id: RCV000054540 RCV004018968
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004579.1:p.Arg28Gln
CA214437
NM_004588.5:c.83G>A