Canonical Allele Identifier: PA2829587141
Gene: MAFB HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005452.2:p.Glu19Gln
CA9857850
NM_005461.5:c.55G>C