Canonical Allele Identifier: PA916045401
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 580052
ClinVar RCV Id: RCV000703482 RCV004026629
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Val1380Ala
CA1943945
NM_001365536.1:c.4139T>C