Canonical Allele Identifier: PA293221
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 138998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_950238.1:p.Leu210Pro
CA293220
NM_199037.5:c.629T>C