Canonical Allele Identifier: PA2826589971
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 1994796
ClinVar RCV Id: RCV002791402
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268652.2:p.Pro321Leu
CA351607806
NM_001281723.3:c.962C>T