Canonical Allele Identifier: PA645406957
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 423904
ClinVar RCV Id: RCV000484447
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Phe207Cys
CA16617259
NM_021007.3:c.620T>G