Canonical Allele Identifier: PA2826591808
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 1901

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268654.1:p.Asp232Gly
CA278012
NM_001281725.2:c.695A>G