Canonical Allele Identifier: PA2826591831
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 551326
ClinVar RCV Id: RCV000666357
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268654.1:p.Tyr241del
CA658822117
NM_001281725.2:c.721_723del