Canonical Allele Identifier: PA645510707
Gene: MMAB HGNC NCBI

Linked Data

ClinVar Variation Id: 439902
ClinVar RCV Id: RCV001829450
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443077.1:p.Glu74Asp
CA386639737
NM_052845.4:c.222A>T
CA386639741
NM_052845.4:c.222A>C