Canonical Allele Identifier: PA2826590562
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25004
ClinVar RCV Id: RCV000021923 RCV000438885 RCV001266904 RCV003904859
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.Pro122Thr
CA278199
NM_001281724.3:c.364C>A