Canonical Allele Identifier: PA2826590058
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 343911
ClinVar RCV Id: RCV000358739
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268652.2:p.Pro372Ser
CA10617574
NM_001281723.3:c.1114C>T