Canonical Allele Identifier: PA2580102800
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 657685
ClinVar RCV Id: RCV000814343
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000051.1:p.Gln80Pro
CA351603644
NM_000060.4:c.239A>C