Canonical Allele Identifier: PA278180
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 24993
ClinVar RCV Id: RCV000021911
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000051.1:p.Tyr93Cys
CA278179
NM_000060.4:c.278A>G