Canonical Allele Identifier: PA2829675821
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 571695
ClinVar RCV Id: RCV000692909
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Phe1319Ser
CA349052909
NM_006920.6:c.3956T>C