Canonical Allele Identifier: PA2828476230
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 801783
ClinVar RCV Id: RCV000986859
ClinVar Variation Id: 801784
ClinVar RCV Id: RCV000986860
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Met1545Ile
CA349036335
NM_001371247.1:c.4635G>A
CA349036336
NM_001371247.1:c.4635G>C
CA349036337
NM_001371247.1:c.4635G>T