Canonical Allele Identifier: PA1139751355
Gene: MMAB HGNC NCBI

Linked Data

ClinVar Variation Id: 989538
ClinVar RCV Id: RCV001277393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443077.1:p.Ser69Thr
CA6779004
NM_052845.4:c.206G>C