Canonical Allele Identifier: PA2826590774
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25036
ClinVar RCV Id: RCV000021958
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.Ala217Thr
CA278250
NM_001281724.3:c.649G>A