Canonical Allele Identifier: PA645415853
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 429499
ClinVar RCV Id: RCV000493721 RCV003766771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001028.1:p.Ala150Val
CA405329894
NM_001037.5:c.449C>T