Canonical Allele Identifier: PA645415999
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 406501
ClinVar RCV Id: RCV000457996

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_950238.1:p.His223Asp
CA9372049
NM_199037.5:c.667C>G