Canonical Allele Identifier: PA2580103051
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 2057329

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000051.1:p.Ala533Val
CA2277500
NM_000060.4:c.1598C>T