Canonical Allele Identifier: PA2741915329
Gene: SCN2B HGNC NCBI
ClinVar RCV:
RCV003882713
ClinVar Variation:
3023527
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004579.1:p.Glu149Gly
CA382784320
NM_004588.5:c.446A>G