Canonical Allele Identifier: PA2580368409
Gene: SCN11A HGNC NCBI

Linked Data

ClinVar Variation Id: 1747031
ClinVar RCV Id: RCV002346991 RCV003439001
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054858.2:p.Gly1786Asp
CA72959127
NM_014139.3:c.5357G>A