Canonical Allele Identifier: PA1139755083
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 975994

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_950238.1:p.Arg191Gln
CA9372037
NM_199037.5:c.572G>A