Canonical Allele Identifier: PA916048699
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 556687
ClinVar RCV Id: RCV000672725
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357682.1:p.Ile87Met
CA70619147
NM_001370753.1:c.261T>G