Canonical Allele Identifier: PA2826589869
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25043
ClinVar RCV Id: RCV000021965
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268652.2:p.Trp252Gly
CA278262
NM_001281723.3:c.754T>G