Canonical Allele Identifier: PA1139738659
Gene: BICD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 954395

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056065.1:p.Ser681Leu
CA374034117
NM_015250.4:c.2042C>T