Canonical Allele Identifier: PA2573097864
Gene: MMAB HGNC NCBI

Linked Data

ClinVar Variation Id: 1306747
ClinVar RCV Id: RCV001770927

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443077.1:p.Ser217Arg
CA386635773
NM_052845.4:c.651T>G
CA386635774
NM_052845.4:c.651T>A
CA386635779
NM_052845.4:c.649A>C