Canonical Allele Identifier: PA2499282920
Gene: EFEMP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1010177
ClinVar RCV Id: RCV001307766

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058634.4:p.Ile259Ala
CA1979444763
NM_016938.5:c.774_776delinsTGC