Canonical Allele Identifier: PA658660310
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 450936
ClinVar RCV Id: RCV000521306 RCV001346848 RCV002481715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_950238.1:p.Pro184Leu
CA9372033
NM_199037.5:c.551C>T