Canonical Allele Identifier: PA2826589839
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25039
ClinVar RCV Id: RCV000021961
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268652.2:p.Pro233Ser
CA278256
NM_001281723.3:c.697C>T