Canonical Allele Identifier: PA278301
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25065
ClinVar RCV Id: RCV000021990 RCV000759002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000051.1:p.Thr404Ile
CA278300
NM_000060.4:c.1211C>T