Canonical Allele Identifier: PA916045408
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 471125
ClinVar RCV Id: RCV000539720
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Leu1397Pro
CA349063220
NM_001365536.1:c.4190T>C