Canonical Allele Identifier: PA2580222222
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 2444752
ClinVar RCV Id: RCV003154155
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Ala718Ser
CA349079851
NM_001365536.1:c.2152G>T