Canonical Allele Identifier: PA2826590572
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 1049760
ClinVar RCV Id: RCV001356279 RCV002476631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.Pro126Arg
CA2277308
NM_001281724.3:c.377C>G