Canonical Allele Identifier: PA916045300
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 6350
ClinVar RCV Id: RCV000006722 RCV001004018 RCV001067998 RCV001270748 RCV001781194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Ile859Thr
CA340545
NM_001365536.1:c.2576T>C