Canonical Allele Identifier: PA2499295281
Gene: MMAB HGNC NCBI

Linked Data

ClinVar Variation Id: 1298554
ClinVar RCV Id: RCV001726884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443077.1:p.Met229Val
CA6778761
NM_052845.4:c.685A>G