Canonical Allele Identifier: PA658827166
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 558593
ClinVar RCV Id: RCV000674889 RCV001844220
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000051.1:p.Leu437Val
CA351608522
NM_000060.4:c.1309C>G