Canonical Allele Identifier: PA2828470271
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1317212
ClinVar RCV Id: RCV001759084
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358175.1:p.Ser13Gly
CA349009731
NM_001371246.1:c.37A>G