Canonical Allele Identifier: PA916048659
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_001357681.1:p.Asp232Gly
CA278012
NM_001370752.1:c.695A>G