Canonical Allele Identifier: PA2827771489
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 93653
ClinVar RCV Id: RCV000723573 RCV001854405
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Asn1517Lys
CA221595
NM_001353951.2:c.4551C>A
CA349072381
NM_001353951.2:c.4551C>G