Canonical Allele Identifier: PA658677186
Gene: MANBA HGNC NCBI

Linked Data

ClinVar Variation Id: 475412
ClinVar RCV Id: RCV000538639

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005899.3:p.Cys761Ser
CA3026657
NM_005908.4:c.2282G>C
CA357756831
NM_005908.4:c.2281T>A