Canonical Allele Identifier: PA2827773315
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 856834
ClinVar RCV Id: RCV001062381
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Thr771Ser
CA349064124
NM_001353952.2:c.2312C>G
CA349064129
NM_001353952.2:c.2311A>T