Canonical Allele Identifier: PA2826832938
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 573935
ClinVar RCV Id: RCV000695738

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280235.2:p.Leu1056Arg
CA352156689
NM_001293306.2:c.3167T>G