Canonical Allele Identifier: PA2829668997
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 965988
ClinVar RCV Id: RCV001240563

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Leu1033Gln
CA2320351
NM_006514.4:c.3098T>A