Canonical Allele Identifier: PA2826592498
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 439037
ClinVar RCV Id: RCV000507334 RCV001348854
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268655.2:p.Pro91Ala
CA351605101
NM_001281726.2:c.271C>G