Canonical Allele Identifier: PA2826592393
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 38483

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268655.2:p.His23Arg
CA278364
NM_001281726.2:c.68A>G