Canonical Allele Identifier: PA205613
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 195797
ClinVar RCV Id: RCV000192652 RCV000276428 RCV000331539 RCV000371033 RCV000356751 RCV000713115 RCV001083289 RCV004537399
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Val1564Ile
CA205612
NM_000334.4:c.4690G>A