Canonical Allele Identifier: PA916051132
Gene: MMAB HGNC NCBI

Linked Data

ClinVar Variation Id: 643413
ClinVar RCV Id: RCV000797106

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443077.1:p.Arg195Cys
CA6778823
NM_052845.4:c.583C>T