Canonical Allele Identifier: PA2827069205
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 436652
ClinVar RCV Id: RCV000503065 RCV000815939 RCV001764493 RCV002476008
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308534.1:p.Arg12Cys
CA9371961
NM_001321605.1:c.34C>T