Canonical Allele Identifier: PA645415901
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_950238.1:p.Asp103Val
CA16044237
NM_199037.5:c.308A>T