Canonical Allele Identifier: PA2826590522
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 24999
ClinVar RCV Id: RCV000021918 RCV000759007 RCV002513162
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.Gly94Val
CA278191
NM_001281724.3:c.281G>T