Canonical Allele Identifier: PA2826591369
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 1897

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.Thr512Met
CA278009
NM_001281724.3:c.1535C>T