Canonical Allele Identifier: PA658679277
Gene: MEGF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 473334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001401.2:p.Leu1694Val
CA9475511
NM_001410.3:c.5080C>G