Allele Registry

Canonical Allele Identifier: PA095967

Gene: MMAB HGNC NCBI

ClinVar RCV:

RCV000202597

RCV000414492

RCV002515492

ClinVar Variation:

218324

HGVS (amino-acid)	Matching Registered Transcripts
NP_443077.1:p.Arg191Trp	CA347810 NM_052845.4:c.571C>T