Canonical Allele Identifier: PA2826591816
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25040
ClinVar RCV Id: RCV000021962
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268654.1:p.Ile235Thr
CA278258
NM_001281725.2:c.704T>C