Canonical Allele Identifier: PA093594
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 1897

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000051.1:p.Thr532Met
CA278009
NM_000060.4:c.1595C>T