Canonical Allele Identifier: PA2827788888
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 421777

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Met1238Thr
CA16617297
NM_001353960.2:c.3713T>C