Canonical Allele Identifier: PA916048613
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 1897

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357587.1:p.Thr512Met
CA278009
NM_001370658.1:c.1535C>T