Canonical Allele Identifier: PA916051087
Gene: MMAB HGNC NCBI
ClinVar RCV:
RCV000202589
ClinVar Variation:
218326
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443077.1:p.Gly97Glu
CA278561
NM_052845.4:c.290G>A