Canonical Allele Identifier: PA143973
Gene: BICD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 55861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001003800.1:p.Lys508Thr
CA143972
NM_001003800.2:c.1523A>C