Canonical Allele Identifier: PA2826923942
Gene: MEGF10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1002633

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295050.1:p.Asn508Ser
CA3391598
NM_001308121.2:c.1523A>G