Canonical Allele Identifier: PA2826591213
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25082

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.Gly425Val
CA278330
NM_001281724.3:c.1274G>T