Canonical Allele Identifier: PA2573314589
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 1371605
ClinVar RCV Id: RCV001879077
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_950238.1:p.Leu180Phe
CA405329263
NM_199037.5:c.538C>T