Canonical Allele Identifier: PA2826398948
Gene: MEGF10 HGNC NCBI

Linked Data

ClinVar Variation Id: 350651
ClinVar RCV Id: RCV000259200 RCV002523500 RCV001706569
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243474.1:p.Gly522Arg
CA3391612
NM_001256545.2:c.1564G>A
CA3391613
NM_001256545.2:c.1564G>C