Canonical Allele Identifier: PA645408082
Gene: SCN3B HGNC NCBI

Linked Data

ClinVar Variation Id: 224720

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060870.1:p.Ile141Met
CA10575989
NM_018400.3:c.423C>G