Canonical Allele Identifier: PA2826590805
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 1901
ClinVar RCV Id: RCV000001978 RCV000445043
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.Asp232Gly
CA278012
NM_001281724.3:c.695A>G