Canonical Allele Identifier: PA2741872768
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 2932498
ClinVar RCV Id: RCV003795712
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Trp1382Arg
CA1943942
NM_001365536.1:c.4144T>A
CA349063440
NM_001365536.1:c.4144T>C