Allele Registry

Canonical Allele Identifier: PA3057354103

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV004954863

ClinVar Variation:

3438233

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Ser682Leu	CA8709666 NM_000334.4:c.2045C>T