Canonical Allele Identifier: PA317998
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 207012
ClinVar RCV Id: RCV000189164 RCV002517894
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Met1545Val
CA317997
NM_001040142.2:c.4633A>G