Canonical Allele Identifier: PA278434
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_000051.1:p.Met86Arg
CA278433
NM_000060.4:c.257T>G