Canonical Allele Identifier: PA2580328688
Gene: MANBA HGNC NCBI
ClinVar RCV:
RCV002690853
ClinVar Variation:
1957738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005899.3:p.Ala19Thr
CA357961625
NM_005908.4:c.55G>A