Canonical Allele Identifier: PA207844
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 212125
ClinVar RCV Id: RCV000193985 RCV000413708 RCV001265401 RCV001390104
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Arg856Gln
CA207842
NM_021007.3:c.2567G>A