ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2828448662
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_001357681.1:p.Leu63_Leu65del
CA278172
NM_001370752.1:c.187_195del