Canonical Allele Identifier: PA347904
Gene: MMAB HGNC NCBI

Linked Data

ClinVar Variation Id: 219007
ClinVar RCV Id: RCV000203386 RCV000424166 RCV002509300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443077.1:p.Tyr219Cys
CA347903
NM_052845.4:c.656A>G