Canonical Allele Identifier: PA916048598
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25108
ClinVar RCV Id: RCV000022034 RCV001266891 RCV002271373 RCV003476902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357587.1:p.Ala458Thr
CA278372
NM_001370658.1:c.1372G>A