Canonical Allele Identifier: PA2826923529
Gene: MEGF10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1372362
ClinVar RCV Id: RCV001872928
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295048.1:p.Cys514Ser
CA360730098
NM_001308119.1:c.1540T>A
CA360730107
NM_001308119.1:c.1541G>C