Canonical Allele Identifier: PA2826589957
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 38278
ClinVar RCV Id: RCV000021978 RCV000622271 RCV000723564 RCV002298452
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268652.2:p.His303Arg
CA220339
NM_001281723.3:c.908A>G