Canonical Allele Identifier: PA2826591851
Gene: BTD HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268654.1:p.Trp252Gly
CA278262
NM_001281725.2:c.754T>G