Canonical Allele Identifier: PA645383910
Gene: BCDIN3D HGNC NCBI

Linked Data

ClinVar Variation Id: 254103
ClinVar RCV Id: RCV000240071 RCV000950779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_859059.1:p.Asp8Gly
CA6558696
NM_181708.3:c.23A>G