Canonical Allele Identifier: PA1139742845
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 941318
ClinVar RCV Id: RCV001211077
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Val992Gly
CA349074632
NM_001365536.1:c.2975T>G