Canonical Allele Identifier: PA2829669015
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 407759

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Gly1051Arg
CA2320339
NM_006514.4:c.3151G>A
CA352156728
NM_006514.4:c.3151G>C