Allele Registry

Canonical Allele Identifier: PA645453471

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV000435175

RCV000821671

ClinVar Variation:

383923

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Leu796Val	CA16607432 NM_000334.4:c.2386C>G