Canonical Allele Identifier: PA2742030249
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 2758106
ClinVar RCV Id: RCV003510090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_950238.1:p.Pro220Ser
CA307703781
NM_199037.5:c.658C>T