Canonical Allele Identifier: PA2825357940
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1342695
ClinVar RCV Id: RCV001847369 RCV002319729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035233.1:p.Thr236Ser
CA349017761
NM_001040143.2:c.706A>T
CA349017766
NM_001040143.2:c.707C>G