Canonical Allele Identifier: PA2825356824
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 548699
ClinVar RCV Id: RCV000662338 RCV001265501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Val1601Leu
CA349036914
NM_001040142.2:c.4801G>C
CA349036915
NM_001040142.2:c.4801G>T