Canonical Allele Identifier: PA2828180692
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 94090
ClinVar RCV Id: RCV000080039 RCV000284177 RCV000389941 RCV000469131 RCV000375717 RCV000490436 RCV000992915
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Val1002Leu
CA147606
NM_001365536.1:c.3004G>T
CA357867
NM_001365536.1:c.[3004G>T;2827A>C]
CA349074509
NM_001365536.1:c.3004G>C