Canonical Allele Identifier: PA658828351
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 546315
ClinVar RCV Id: RCV000658172
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Asn1561Lys
CA349036491
NM_021007.3:c.4683C>A
CA349036492
NM_021007.3:c.4683C>G