Canonical Allele Identifier: PA278849
Gene: MAF HGNC NCBI

Linked Data

ClinVar Variation Id: 217344
ClinVar RCV Id: RCV000203408
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005351.2:p.Arg294Trp
CA278847
NM_005360.5:c.880C>T