Canonical Allele Identifier: PA2828445784
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25001

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357587.1:p.Arg102Gly
CA278195
NM_001370658.1:c.304A>G