Canonical Allele Identifier: PA2827787392
Gene: SCN1A HGNC NCBI
ClinVar RCV:
RCV000180856
ClinVar Variation:
189904
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Gly177Val
CA303263
NM_001353960.2:c.530G>T