Canonical Allele Identifier: PA916005280
Gene: MEGF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 473334
ClinVar RCV Id: RCV000527674 RCV002530218
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258867.1:p.Leu1761Val
CA9475511
NM_001271938.2:c.5281C>G