Allele Registry

Canonical Allele Identifier: PA285092

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059478

RCV000519717

RCV003992313

ClinVar Variation:

68601

451108

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.His928Gln	CA285090 NM_006920.6:c.2784C>G CA349061306 NM_006920.6:c.2784C>A