Canonical Allele Identifier: PA2829669004
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 2621908
ClinVar RCV Id: RCV004363681

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Asp1041Glu
CA352156782
NM_006514.4:c.3123C>G
CA352156783
NM_006514.4:c.3123C>A