Canonical Allele Identifier: PA2826590138
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 1525004
ClinVar RCV Id: RCV002049719
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268652.2:p.Glu409Ala
CA351608471
NM_001281723.3:c.1226A>C