Canonical Allele Identifier: PA2580328687
Gene: MANBA HGNC NCBI

Linked Data

ClinVar Variation Id: 1997022
ClinVar RCV Id: RCV002823884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005899.3:p.Gly13Ser
CA357961658
NM_005908.4:c.37G>A