Canonical Allele Identifier: PA112568
Gene: MEGF10 HGNC NCBI

Linked Data

ClinVar Variation Id: 30966
ClinVar RCV Id: RCV000023957 RCV001385515
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243474.1:p.Cys326Arg
CA129574
NM_001256545.2:c.976T>C