Canonical Allele Identifier: PA2826590177
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25082
ClinVar RCV Id: RCV000022007 RCV000985644
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268652.2:p.Gly425Val
CA278330
NM_001281723.3:c.1274G>T