Canonical Allele Identifier: PA130633
Gene: MEGF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 39845
ClinVar RCV Id: RCV000033072
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001401.2:p.Arg1499His
CA130632
NM_001410.3:c.4496G>A