ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA209997
Gene: SCN2A
HGNC
NCBI
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_066287.2:p.Ser987Ile
CA209995
NM_021007.3:c.2960G>T