Canonical Allele Identifier: PA302164
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 190864

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_950238.1:p.Ser198Gly
CA302163
NM_199037.5:c.592A>G