Canonical Allele Identifier: PA2826591302
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 1903

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.Asn469Thr
CA278014
NM_001281724.3:c.1406A>C