Canonical Allele Identifier: PA2828180495
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 331988
ClinVar RCV Id: RCV000293514 RCV000363472 RCV000346132 RCV000401490 RCV000493503 RCV000688718
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Arg540His
CA1944463
NM_001365536.1:c.1619G>A