Canonical Allele Identifier: PA2580102879
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 809437
ClinVar RCV Id: RCV000998008
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000051.1:p.Val267Leu
CA351607248
NM_000060.4:c.799G>T
CA351607249
NM_000060.4:c.799G>C