Canonical Allele Identifier: PA915978598
Gene: BICD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 208737
ClinVar RCV Id: RCV000190756
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056065.1:p.Phe530Ser
CA204791
NM_015250.4:c.1589T>C