Canonical Allele Identifier: PA2580493369
Gene: MMAB HGNC NCBI

Linked Data

ClinVar Variation Id: 2143011
ClinVar RCV Id: RCV003076510
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443077.1:p.Lys230Thr
CA6778760
NM_052845.4:c.689A>C