Canonical Allele Identifier: PA2742030244
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 2718773
ClinVar RCV Id: RCV003511005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_950238.1:p.Ser211Tyr
CA405329526
NM_199037.5:c.632C>A