Canonical Allele Identifier: PA2826591774
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25036
ClinVar RCV Id: RCV000021958
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268654.1:p.Ala217Thr
CA278250
NM_001281725.2:c.649G>A