Canonical Allele Identifier: PA2741872627
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 2923349
ClinVar RCV Id: RCV003780467
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Ser1065Arg
CA349073252
NM_001365536.1:c.3195C>G
CA349073255
NM_001365536.1:c.3195C>A
CA349073268
NM_001365536.1:c.3193A>C