Canonical Allele Identifier: PA645453504
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 324525
ClinVar RCV Id: RCV000270326 RCV000271110 RCV000332377 RCV000362158 RCV000555752 RCV002280115 RCV004537817
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Val999Met
CA8709421
NM_000334.4:c.2995G>A