Canonical Allele Identifier: PA2826832922
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 3023103
ClinVar RCV Id: RCV003882289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280235.2:p.Cys1038Phe
CA352156798
NM_001293306.2:c.3113G>T