Canonical Allele Identifier: PA1139751569
Gene: MMAB HGNC NCBI

Linked Data

ClinVar Variation Id: 881084
ClinVar RCV Id: RCV001109832
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443077.1:p.Asp218Glu
CA243447483
NM_052845.4:c.654C>G
CA386635760
NM_052845.4:c.654C>A