Canonical Allele Identifier: PA2825361280
Gene: SCN3B HGNC NCBI

Linked Data

ClinVar Variation Id: 190888

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035241.1:p.Arg139Gln
CA302210
NM_001040151.2:c.416G>A