Canonical Allele Identifier: PA2826923851
Gene: MEGF10 HGNC NCBI

Linked Data

ClinVar Variation Id: 30966

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295050.1:p.Cys326Arg
CA129574
NM_001308121.2:c.976T>C