Canonical Allele Identifier: PA2826590168
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 289111
ClinVar RCV Id: RCV000293118 RCV001036979
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268652.2:p.Val422Ile
CA2277457
NM_001281723.3:c.1264G>A