Canonical Allele Identifier: PA2826590884
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 379232

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.Ala269Val
CA16604827
NM_001281724.3:c.806C>T