Canonical Allele Identifier: PA2499304115
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 1216107

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_950238.1:p.Gly227Arg
CA405329620
NM_199037.5:c.679G>C
CA405329622
NM_199037.5:c.679G>A