Canonical Allele Identifier: PA2826592421
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 38574

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268655.2:p.Glu44Asp
CA278386
NM_001281726.2:c.132G>C
CA351603230
NM_001281726.2:c.132G>T