Canonical Allele Identifier: PA913197552
Gene: MAFB HGNC NCBI

Linked Data

ClinVar Variation Id: 593578
ClinVar RCV Id: RCV000728664 RCV002493309
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005452.2:p.Pro42Leu
CA408941831
NM_005461.5:c.125C>T