Canonical Allele Identifier: PA2826591517
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 556687
ClinVar RCV Id: RCV000672725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268654.1:p.Ile87Met
CA70619147
NM_001281725.2:c.261T>G