Canonical Allele Identifier: PA2829856930
Gene: EFEMP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3226940
ClinVar RCV Id: RCV004522106
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058634.4:p.Val316Met
CA6110473
NM_016938.5:c.946G>A