Canonical Allele Identifier: PA2826592537
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25004
ClinVar RCV Id: RCV000021923 RCV000438885 RCV001266904 RCV003904859
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268655.2:p.Pro122Thr
CA278199
NM_001281726.2:c.364C>A