Allele Registry

Canonical Allele Identifier: PA2573240609

Gene: MANBA HGNC NCBI

ClinVar RCV:

RCV002029192

ClinVar Variation:

1514244

HGVS (amino-acid)	Matching Registered Transcripts
NP_005899.3:p.Thr701Arg	CA3026715 NM_005908.4:c.2102C>G