Canonical Allele Identifier: PA2499304116
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 1023790
ClinVar RCV Id: RCV001323895
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_950238.1:p.Arg229Thr
CA405329636
NM_199037.5:c.686G>C