Canonical Allele Identifier: PA2828448636
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 38482
ClinVar RCV Id: RCV000021900 RCV000427971
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357681.1:p.Leu51Pro
CA278161
NM_001370752.1:c.152T>C