Canonical Allele Identifier: PA2825361285
Gene: SCN3B HGNC NCBI

Linked Data

ClinVar Variation Id: 224720

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035241.1:p.Ile141Met
CA10575989
NM_001040151.2:c.423C>G