Canonical Allele Identifier: PA1139742825
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 944391
ClinVar RCV Id: RCV001214781
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Lys893Arg
CA59794652
NM_001365536.1:c.2678A>G