Canonical Allele Identifier: PA2825028154
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 1984039
ClinVar RCV Id: RCV002775298
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000051.1:p.Asp104Gly
CA351605019
NM_000060.4:c.311A>G