Canonical Allele Identifier: PA2826591219
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25083
ClinVar RCV Id: RCV000022008
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.His427Tyr
CA278332
NM_001281724.3:c.1279C>T