Canonical Allele Identifier: PA2828445700
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 2501355
ClinVar RCV Id: RCV003227150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357587.1:p.Ala55Ser
CA351603450
NM_001370658.1:c.163G>T