Canonical Allele Identifier: PA2828475543
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 432058
ClinVar RCV Id: RCV000497729 RCV000623062
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Leu1242Phe
CA349027759
NM_001371247.1:c.3726A>C
CA349027760
NM_001371247.1:c.3726A>T