Canonical Allele Identifier: PA2741872999
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 2949263
ClinVar RCV Id: RCV003801989
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Arg1973Gly
CA349051074
NM_001365536.1:c.5917A>G