Canonical Allele Identifier: PA916048628
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25014
ClinVar RCV Id: RCV000021934
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357681.1:p.Ala142Val
CA278217
NM_001370752.1:c.425C>T