Canonical Allele Identifier: PA2580103009
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 619667
ClinVar RCV Id: RCV000759004
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000051.1:p.Gly451Val
CA351608606
NM_000060.4:c.1352G>T