Allele Registry

Canonical Allele Identifier: PA129573

Gene: MEGF10 HGNC NCBI

ClinVar Allele:

39922

ClinVar RCV:

RCV000023955

RCV000023956

RCV003156219

ClinVar Variation:

30965

HGVS (amino-acid)	Matching Registered Transcripts
NP_115822.1:p.Cys774Arg	CA129572 NM_032446.3:c.2320T>C