Canonical Allele Identifier: PA2580189457
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1728045
ClinVar RCV Id: RCV002320677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280236.2:p.Ser949Gly
CA352156751
NM_001293307.2:c.2845A>G