Canonical Allele Identifier: PA2826591078
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 2439581
ClinVar RCV Id: RCV003143832
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.Pro372del
CA2580614150
NM_001281724.3:c.1113_1115del