Canonical Allele Identifier: PA2826589467
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 38487
ClinVar RCV Id: RCV000021895
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268652.2:p.Val42Met
CA278152
NM_001281723.3:c.124G>A