Canonical Allele Identifier: PA2826832923
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 2621908
ClinVar RCV Id: RCV004363681

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280235.2:p.Asp1040Glu
CA352156782
NM_001293306.2:c.3120C>G
CA352156783
NM_001293306.2:c.3120C>A