Canonical Allele Identifier: PA2826589987
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25107
ClinVar RCV Id: RCV000022033 RCV000278976
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268652.2:p.Asn329Thr
CA278370
NM_001281723.3:c.986A>C