Canonical Allele Identifier: PA2826590981
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 1942484
ClinVar RCV Id: RCV002646822
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.Val322Ala
CA2277407
NM_001281724.3:c.965T>C