Canonical Allele Identifier: PA2827195649
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 1365614
ClinVar RCV Id: RCV001929892 RCV003155434
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310511.1:p.Leu63_Leu65del
CA278172
NM_001323582.1:c.187_195del