Canonical Allele Identifier: PA2826398921
Gene: MEGF10 HGNC NCBI

Linked Data

ClinVar Variation Id: 350650

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243474.1:p.Gly479Arg
CA3391583
NM_001256545.2:c.1435G>A
CA360729827
NM_001256545.2:c.1435G>C