Canonical Allele Identifier: PA093543
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 1900

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000051.1:p.Asp444His
CA090886
NM_000060.4:c.1330G>C