Canonical Allele Identifier: PA2826590807
Gene: BTD HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.Pro233Ser
CA278256
NM_001281724.3:c.697C>T