Canonical Allele Identifier: PA2825353750
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 449583
ClinVar RCV Id: RCV000523254 RCV001309572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Phe307Leu
CA349018607
NM_001040142.2:c.919T>C
CA349018611
NM_001040142.2:c.921C>A
CA349018612
NM_001040142.2:c.921C>G