Canonical Allele Identifier: PA2828473861
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1420984
ClinVar RCV Id: RCV001943689
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Asn212Ser
CA349017401
NM_001371247.1:c.635A>G