Canonical Allele Identifier: PA2825259253
Gene: BICD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1806728
ClinVar RCV Id: RCV002474157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001003800.1:p.Cys437Ser
CA374038973
NM_001003800.2:c.1310G>C
CA374038977
NM_001003800.2:c.1309T>A