Canonical Allele Identifier: PA2826589645
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 38290
ClinVar RCV Id: RCV000021904 RCV000078072
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268652.2:p.Arg137His
CA220323
NM_001281723.3:c.410G>A