Canonical Allele Identifier: PA658660965
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 464920
ClinVar RCV Id: RCV000533201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Ser229Ala
CA349017594
NM_021007.3:c.685T>G