Canonical Allele Identifier: PA2828448668
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 156000
ClinVar RCV Id: RCV000144056 RCV003323415
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357681.1:p.Met66Arg
CA278433
NM_001370752.1:c.197T>G