Canonical Allele Identifier: PA2828180699
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 331974
ClinVar RCV Id: RCV000308517 RCV000333798 RCV000330258 RCV000368610 RCV000865153 RCV001705501 RCV000478443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Arg1007His
CA1944153
NM_001365536.1:c.3020G>A