Canonical Allele Identifier: PA658660291
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 470177
ClinVar RCV Id: RCV000548321
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_950238.1:p.Arg96Trp
CA9372001
NM_199037.5:c.286C>T