Canonical Allele Identifier: PA2828445740
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 1984039
ClinVar RCV Id: RCV002775298

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357587.1:p.Asp84Gly
CA351605019
NM_001370658.1:c.251A>G