Canonical Allele Identifier: PA2829669019
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 573935
ClinVar RCV Id: RCV000695738

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Leu1057Arg
CA352156689
NM_006514.4:c.3170T>G