Canonical Allele Identifier: PA2826832934
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 407759

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280235.2:p.Gly1050Arg
CA2320339
NM_001293306.2:c.3148G>A
CA352156728
NM_001293306.2:c.3148G>C