Canonical Allele Identifier: PA2828180489
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 538480
ClinVar RCV Id: RCV000647800 RCV000757742 RCV000765527 RCV001809733 RCV004025745
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Ser535Leu
CA1944468
NM_001365536.1:c.1604C>T