Canonical Allele Identifier: PA916045271
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 289843
ClinVar RCV Id: RCV000726385 RCV000806907 RCV002429233
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Ile740Met
CA1944308
NM_001365536.1:c.2220T>G