Canonical Allele Identifier: PA916045332
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 569835
ClinVar RCV Id: RCV000690559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Ala1044Gly
CA349073721
NM_001365536.1:c.3131C>G