Canonical Allele Identifier: PA2826590502
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 1984039
ClinVar RCV Id: RCV002775298

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.Asp84Gly
CA351605019
NM_001281724.3:c.251A>G