Canonical Allele Identifier: PA2826592447
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 657685
ClinVar RCV Id: RCV000814343
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268655.2:p.Gln60Pro
CA351603644
NM_001281726.2:c.179A>C