Allele Registry

Canonical Allele Identifier: PA658800671

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV000654699

RCV003488770

ClinVar Variation:

543829

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Met1808Ile	CA8708757 NM_000334.4:c.5424G>A CA400610298 NM_000334.4:c.5424G>T CA400610299 NM_000334.4:c.5424G>C