Allele Registry

Canonical Allele Identifier: PA095962

Gene: MMAB HGNC NCBI

ClinVar RCV:

RCV000203394

RCV000482151

RCV002271462

RCV003967547

ClinVar Variation:

219005

HGVS (amino-acid)	Matching Registered Transcripts
NP_443077.1:p.Ala135Thr	CA347906 NM_052845.4:c.403G>A