Allele Registry

Canonical Allele Identifier: PA095987

Gene: MMAB HGNC NCBI

ClinVar RCV:

RCV000202588

ClinVar Variation:

218323

HGVS (amino-acid)	Matching Registered Transcripts
NP_443077.1:p.Ile96Thr	CA347809 NM_052845.4:c.287T>C