Canonical Allele Identifier: PA281917
Gene: EFEMP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 39012
ClinVar RCV Id: RCV000032270 RCV000033126
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058634.4:p.Glu126Val
CA281916
NM_016938.5:c.377A>T