Allele Registry

Canonical Allele Identifier: PA112577

Gene: MEGF10 HGNC NCBI

ClinVar RCV:

RCV000023955

RCV000023956

RCV003156219

ClinVar Variation:

30965

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243474.1:p.Cys774Arg	CA129572 NM_001256545.2:c.2320T>C