Canonical Allele Identifier: PA093213
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 5902
ClinVar RCV Id: RCV000006263 RCV000206954 RCV000713092 RCV001254163
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Arg675Trp
CA117839
NM_000334.4:c.2023C>T