Canonical Allele Identifier: PA2827195810
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 2734453
ClinVar RCV Id: RCV003499926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310511.1:p.Val237Asp
CA351607167
NM_001323582.1:c.710T>A