Canonical Allele Identifier: PA155060
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 130219
ClinVar RCV Id: RCV000118255 RCV000427650 RCV000330573 RCV001083230 RCV002490810 RCV002312494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Lys908Arg
CA155058
NM_021007.3:c.2723A>G