Canonical Allele Identifier: PA2826590426
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 2918707
ClinVar RCV Id: RCV003601990
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.Val42Ala
CA2277257
NM_001281724.3:c.125T>C