Canonical Allele Identifier: PA2573240540
Gene: MANBA HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005899.3:p.Thr17Ile
CA3027344
NM_005908.4:c.50C>T