Canonical Allele Identifier: PA302212
Gene: SCN3B HGNC NCBI

Linked Data

ClinVar Variation Id: 190888

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060870.1:p.Arg139Gln
CA302210
NM_018400.3:c.416G>A