Canonical Allele Identifier: PA2741915331
Gene: SCN2B HGNC NCBI
ClinVar RCV:
RCV003582467
ClinVar Variation:
2713121
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004579.1:p.Gly168Cys
CA6300419
NM_004588.5:c.502G>T