Allele Registry

Canonical Allele Identifier: PA2741895981

Gene: SCN7A HGNC NCBI

ClinVar RCV:

RCV003982223

ClinVar Variation:

3060194

HGVS (amino-acid)	Matching Registered Transcripts
NP_002967.2:p.Thr41Asn	CA1946017 NM_002976.4:c.122C>A