Canonical Allele Identifier: PA1139714566
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 848680
ClinVar RCV Id: RCV001052491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Val126Ala
CA349076768
NM_006920.6:c.377T>C