Canonical Allele Identifier: PA2828180362
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 1425306
ClinVar RCV Id: RCV001924424
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Asn409Lys
CA349085838
NM_001365536.1:c.1227C>G
CA349085839
NM_001365536.1:c.1227C>A