Canonical Allele Identifier: PA2826589514
Gene: BTD HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268652.2:p.Leu63Ser
CA278175
NM_001281723.3:c.188T>C