Canonical Allele Identifier: PA2580222291
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 2055400
ClinVar RCV Id: RCV002947237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Asp1390Asn
CA1943938
NM_001365536.1:c.4168G>A