Canonical Allele Identifier: PA2826590219
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 641268
ClinVar RCV Id: RCV000794472
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268652.2:p.Gly445Val
CA351608753
NM_001281723.3:c.1334G>T