Canonical Allele Identifier: PA916048702
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_001357682.1:p.Pro91Ala
CA351605101
NM_001370753.1:c.271C>G