Canonical Allele Identifier: PA2826590462
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 1365614
ClinVar RCV Id: RCV001929892 RCV003155434
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.Leu63_Leu65del
CA278172
NM_001281724.3:c.187_195del