Canonical Allele Identifier: PA2499295280
Gene: MMAB HGNC NCBI

Linked Data

ClinVar Variation Id: 1174001
ClinVar RCV Id: RCV001527456
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443077.1:p.Ser217Ile
CA386635775
NM_052845.4:c.650G>T