Canonical Allele Identifier: PA113102
Gene: MEGF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 39846
ClinVar RCV Id: RCV000033073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258867.1:p.Ser2434Gly
CA130634
NM_001271938.2:c.7300A>G