Allele Registry

Canonical Allele Identifier: PA223863

Gene: MMAB HGNC NCBI

ClinVar RCV:

RCV000203347

RCV000790778

ClinVar Variation:

96244

HGVS (amino-acid)	Matching Registered Transcripts
NP_443077.1:p.Arg190Cys	CA223862 NM_052845.4:c.568C>T