Canonical Allele Identifier: PA2829587257
Gene: MAFB HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005452.2:p.Arg289Cys
CA9857743
NM_005461.5:c.865C>T