Canonical Allele Identifier: PA2826590963
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 38278
ClinVar RCV Id: RCV000021978 RCV000622271 RCV000723564 RCV002298452
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.His303Arg
CA220339
NM_001281724.3:c.908A>G