Canonical Allele Identifier: PA130635
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_001401.2:p.Ser2367Gly
CA130634
NM_001410.3:c.7099A>G