Canonical Allele Identifier: PA2499253451
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 1040681
ClinVar RCV Id: RCV001344360 RCV003136007
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Glu1369Lys
CA349063585
NM_001365536.1:c.4105G>A