Canonical Allele Identifier: PA2573240544
Gene: MANBA HGNC NCBI

Linked Data

ClinVar Variation Id: 1418128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005899.3:p.Gly42Arg
CA3027333
NM_005908.4:c.124G>A
CA3027334
NM_005908.4:c.124G>C