Canonical Allele Identifier: PA658811186
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 537732
ClinVar RCV Id: RCV000646747

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_950238.1:p.Arg225His
CA9372052
NM_199037.5:c.674G>A