Canonical Allele Identifier: PA645400391
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 282707
ClinVar RCV Id: RCV000403112 RCV000725125 RCV001053352 RCV002480006
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Arg571Cys
CA5252673
NM_001114753.3:c.1711C>T