Canonical Allele Identifier: PA2827789571
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 408926
ClinVar RCV Id: RCV000460126
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Met1635Thr
CA16610239
NM_001353960.2:c.4904T>C