Canonical Allele Identifier: PA2825353729
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 533491
ClinVar RCV Id: RCV000640622 RCV000658279
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Pro283Ala
CA1939705
NM_001040142.2:c.847C>G