Canonical Allele Identifier: PA2580102934
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 742653
ClinVar RCV Id: RCV000918930

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000051.1:p.Glu353Lys
CA2277413
NM_000060.4:c.1057G>A