Allele Registry

Canonical Allele Identifier: PA100576

Gene: EFEMP2 HGNC NCBI

ClinVar RCV:

RCV000023384

RCV000032274

ClinVar Variation:

39016

HGVS (amino-acid)	Matching Registered Transcripts
NP_058634.4:p.Cys267Tyr	CA281758 NM_016938.5:c.800G>A