Canonical Allele Identifier: PA916005324
Gene: MEGF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 235520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258867.1:p.Pro2558Leu
CA9476230
NM_001271938.2:c.7673C>T