Canonical Allele Identifier: PA1139699222
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 844925
ClinVar RCV Id: RCV001047893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280236.2:p.Ser949Thr
CA352156749
NM_001293307.2:c.2846G>C