Canonical Allele Identifier: PA2826591029
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 664167
ClinVar RCV Id: RCV000822202 RCV001759616
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.Asp348Asn
CA2277423
NM_001281724.3:c.1042G>A