Canonical Allele Identifier: PA2826592157
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 2744068
ClinVar RCV Id: RCV003497656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268654.1:p.Tyr418His
CA351608527
NM_001281725.2:c.1252T>C