Canonical Allele Identifier: PA2826590471
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 156000
ClinVar RCV Id: RCV000144056 RCV003323415
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.Met66Arg
CA278433
NM_001281724.3:c.197T>G