Canonical Allele Identifier: PA1139751378
Gene: MMAB HGNC NCBI

Linked Data

ClinVar Variation Id: 840395
ClinVar RCV Id: RCV001042369

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443077.1:p.Val86Met
CA6778998
NM_052845.4:c.256G>A