Canonical Allele Identifier: PA2499253431
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 1023125
ClinVar RCV Id: RCV001323128
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Gly1049Ser
CA1944132
NM_001365536.1:c.3145G>A