Canonical Allele Identifier: PA916056302
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 224078
ClinVar RCV Id: RCV000209946 RCV001265281
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Gly1576Arg
CA354201
NM_021007.3:c.4726G>A
CA349036640
NM_021007.3:c.4726G>C