Allele Registry

Canonical Allele Identifier: PA2741896049

Gene: SCN7A HGNC NCBI

ClinVar RCV:

RCV003974658

ClinVar Variation:

3059687

HGVS (amino-acid)	Matching Registered Transcripts
NP_002967.2:p.Met958Ile	CA1945357 NM_002976.4:c.2874G>T CA349084467 NM_002976.4:c.2874G>C CA349084469 NM_002976.4:c.2874G>A