Canonical Allele Identifier: PA2828445865
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 38298
ClinVar RCV Id: RCV000031859 RCV000078073 RCV002514126
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357587.1:p.Ala151Thr
CA285305
NM_001370658.1:c.451G>A