Canonical Allele Identifier: PA278299
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25062
ClinVar RCV Id: RCV000021987 RCV000405919 RCV002281714
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000051.1:p.Asn402Ser
CA278298
NM_000060.4:c.1205A>G