Canonical Allele Identifier: PA915978696
Gene: BICD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 155729

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056065.1:p.Val665Leu
CA233053
NM_015250.4:c.1993G>T
CA374034539
NM_015250.4:c.1993G>C