Canonical Allele Identifier: PA2826923929
Gene: MEGF10 HGNC NCBI

Linked Data

ClinVar Variation Id: 906481
ClinVar RCV Id: RCV001155676
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295050.1:p.His478Leu
CA360729824
NM_001308121.2:c.1433A>T