Allele Registry

Canonical Allele Identifier: PA645504279

Gene: MANBA HGNC NCBI

ClinVar RCV:

RCV000354084

RCV000454742

RCV000675791

ClinVar Variation:

347096

HGVS (amino-acid)	Matching Registered Transcripts
NP_005899.3:p.Val253Ile	CA3027113 NM_005908.4:c.757G>A