Canonical Allele Identifier: PA2826590786
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 38281
ClinVar RCV Id: RCV000021959 RCV000724643
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.Cys225Tyr
CA278252
NM_001281724.3:c.674G>A