Canonical Allele Identifier: PA658827157
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 551326
ClinVar RCV Id: RCV000666357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000051.1:p.Tyr261del
CA658822117
NM_000060.4:c.781_783del