Allele Registry

Canonical Allele Identifier: PA2827788436

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059478

RCV000519717

RCV003992313

ClinVar Variation:

68601

451108

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340889.1:p.His910Gln	CA285090 NM_001353960.2:c.2730C>G CA349061306 NM_001353960.2:c.2730C>A