Canonical Allele Identifier: PA2580222292
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 1975275
ClinVar RCV Id: RCV002755594
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Gly1395Arg
CA349063257
NM_001365536.1:c.4183G>C