Canonical Allele Identifier: PA2825358950
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 206969
ClinVar RCV Id: RCV000578274 RCV001265498
ClinVar Variation Id: 2114224
ClinVar RCV Id: RCV003042677
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035233.1:p.Gly879Arg
CA317877
NM_001040143.2:c.2635G>A
CA349013421
NM_001040143.2:c.2635G>C
CA2580064222
NM_001040143.2:c.2634_2635delinsTC