Canonical Allele Identifier: PA2499282928
Gene: EFEMP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1016757
ClinVar RCV Id: RCV001315810
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058634.4:p.Gly407Val
CA381349365
NM_016938.5:c.1220G>T