Canonical Allele Identifier: PA2829669009
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1359668
ClinVar RCV Id: RCV001904483

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Pro1045Arg
CA352156762
NM_006514.4:c.3134C>G