Canonical Allele Identifier: PA2826590983
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 2043400
ClinVar RCV Id: RCV002912966
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.Gly323Val
CA2277409
NM_001281724.3:c.968G>T