Canonical Allele Identifier: PA2826589503
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 657685
ClinVar RCV Id: RCV000814343
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268652.2:p.Gln60Pro
CA351603644
NM_001281723.3:c.179A>C