Canonical Allele Identifier: PA645453757
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 324508
ClinVar RCV Id: RCV000290622 RCV000345319 RCV000384970 RCV000393903 RCV000813822
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Gly1762Arg
CA8708790
NM_000334.4:c.5284G>A
CA400613025
NM_000334.4:c.5284G>C