Canonical Allele Identifier: PA2826590398
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 38483
ClinVar RCV Id: RCV000022030 RCV001251701 RCV002513289
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.His23Arg
CA278364
NM_001281724.3:c.68A>G