Canonical Allele Identifier: PA2827780531
Gene: SCN1A HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Val1577Gly
CA303511
NM_001353955.2:c.4730T>G