Allele Registry

Canonical Allele Identifier: PA645453445

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV000440430

ClinVar Variation:

391923

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Phe671Leu	CA16607817 NM_000334.4:c.2011T>C CA400631572 NM_000334.4:c.2013C>G CA400631574 NM_000334.4:c.2013C>A