Canonical Allele Identifier: PA2826923938
Gene: MEGF10 HGNC NCBI

Linked Data

ClinVar Variation Id: 2208762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295050.1:p.Asn503Ser
CA3391594
NM_001308121.2:c.1508A>G