Canonical Allele Identifier: PA2580159886
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_001135821.1:p.Asp15His
CA382778113
NM_001142349.2:c.43G>C