Canonical Allele Identifier: PA093257
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 5920
ClinVar RCV Id: RCV000489251 RCV000552020 RCV001799588 RCV001823093 RCV002225070 RCV002490328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Gly1306Glu
CA117852
NM_000334.4:c.3917G>A