Canonical Allele Identifier: PA2830374252
Gene: SCN4B HGNC NCBI

Linked Data

ClinVar Variation Id: 1734465
ClinVar RCV Id: RCV002349231
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_777594.1:p.Asp125His
CA382778113
NM_174934.4:c.373G>C