Allele Registry

Canonical Allele Identifier: PA2573168236

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV002007313

ClinVar Variation:

1451612

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Arg1448Gly	CA400616190 NM_000334.4:c.4342C>G