Canonical Allele Identifier: PA2742030251
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 3011809
ClinVar RCV Id: RCV003872872

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_950238.1:p.Pro220Thr
CA405329581
NM_199037.5:c.658C>A