Canonical Allele Identifier: PA2827069497
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 429499
ClinVar RCV Id: RCV000493721 RCV003766771
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308534.1:p.Ala117Val
CA405329894
NM_001321605.1:c.350C>T