Canonical Allele Identifier: PA916048680
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25048
ClinVar RCV Id: RCV001310478 RCV003323364 RCV003497832
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357681.1:p.Val276Gly
CA278272
NM_001370752.1:c.827T>G