Canonical Allele Identifier: PA093439
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 5896
ClinVar RCV Id: RCV000006254 RCV000006255 RCV000255373 RCV000763020 RCV003231090 RCV002291266 RCV004532296
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Thr704Met
CA117833
NM_000334.4:c.2111C>T