Canonical Allele Identifier: PA2826590905
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25048
ClinVar RCV Id: RCV001310478 RCV003323364 RCV003497832
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.Val276Gly
CA278272
NM_001281724.3:c.827T>G