Canonical Allele Identifier: PA2825259193
Gene: BICD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1662339

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001003800.1:p.Arg398Trp
CA5126612
NM_001003800.2:c.1192C>T