Canonical Allele Identifier: PA2573240540
Gene: MANBA HGNC NCBI

Linked Data

ClinVar Variation Id: 1434532
ClinVar RCV Id: RCV001962462
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005899.3:p.Thr17Ile
CA3027344
NM_005908.4:c.50C>T