Canonical Allele Identifier: PA916061750
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 9255
ClinVar RCV Id: RCV000009837 RCV003332078 RCV003988820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_950238.1:p.Glu87Gln
CA120244
NM_199037.5:c.259G>C