Canonical Allele Identifier: PA1139741999
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 984860
ClinVar RCV Id: RCV001265408 RCV003770378
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Gly211Asp
CA349017386
NM_021007.3:c.632G>A