Canonical Allele Identifier: PA915978591
Gene: BICD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 578721
ClinVar RCV Id: RCV000701818
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056065.1:p.Ser521Gly
CA374037275
NM_015250.4:c.1561A>G