Canonical Allele Identifier: PA2499282913
Gene: EFEMP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1000032
ClinVar RCV Id: RCV001296107

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058634.4:p.Ile72Thr
CA381310340
NM_016938.5:c.215T>C