ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827761487
Gene: SCN1A
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000188998
RCV001065456
RCV003156083
ClinVar Variation:
206863
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001340878.1:p.Phe1753Tyr
CA317597
NM_001353949.2:c.5258T>A