Canonical Allele Identifier: PA2580102930
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 2043400
ClinVar RCV Id: RCV002912966

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000051.1:p.Gly343Val
CA2277409
NM_000060.4:c.1028G>T