Canonical Allele Identifier: PA1139742846
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 943117
ClinVar RCV Id: RCV001213244 RCV002436821
ClinVar Variation Id: 1929737
ClinVar RCV Id: RCV002626446
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Lys997Asn
CA1944158
NM_001365536.1:c.2991G>T
CA349074557
NM_001365536.1:c.2991G>C