Canonical Allele Identifier: PA2826592053
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 651913
ClinVar RCV Id: RCV000807358
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268654.1:p.Thr373del
CA1139655729
NM_001281725.2:c.1116_1118del