ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827771449
Gene: SCN1A
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000487743
RCV001328670
RCV001385358
ClinVar Variation:
425224
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001340880.1:p.Ala1499Val
CA16621765
NM_001353951.2:c.4496C>T