Canonical Allele Identifier: PA2826590898
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25047
ClinVar RCV Id: RCV000021969 RCV000224487 RCV002265566 RCV003964809
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.Ile274Val
CA278270
NM_001281724.3:c.820A>G