Canonical Allele Identifier: PA2826832544
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 2448845
ClinVar RCV Id: RCV003168386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280235.2:p.Gln570Lys
CA352167162
NM_001293306.2:c.1708C>A