Allele Registry

Canonical Allele Identifier: PA358790

Gene: MMAB HGNC NCBI

ClinVar RCV:

RCV000210838

ClinVar Variation:

225186

HGVS (amino-acid)	Matching Registered Transcripts
NP_443077.1:p.Val188Gly	CA358789 NM_052845.4:c.563T>G