Canonical Allele Identifier: PA093526
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 1898

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000051.1:p.Arg538Cys
CA220320
NM_000060.4:c.1612C>T