Allele Registry

Canonical Allele Identifier: PA916010528

Gene: SCN11A HGNC NCBI

ClinVar RCV:

RCV000074495

RCV001229351

RCV002514311

RCV003886374

ClinVar Variation:

69850

HGVS (amino-acid)	Matching Registered Transcripts
NP_054858.2:p.Arg225Cys	CA145434 NM_014139.3:c.673C>T