Canonical Allele Identifier: PA2828448969
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 38281
ClinVar RCV Id: RCV000021959 RCV000724643
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357681.1:p.Cys225Tyr
CA278252
NM_001370752.1:c.674G>A