Canonical Allele Identifier: PA916018825
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 573935
ClinVar RCV Id: RCV000695738

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280236.2:p.Leu959Arg
CA352156689
NM_001293307.2:c.2876T>G