Canonical Allele Identifier: PA916025084
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 375404
ClinVar RCV Id: RCV000416448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308534.1:p.Asp70Val
CA16044237
NM_001321605.1:c.209A>T