Canonical Allele Identifier: PA101041
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 213212
ClinVar RCV Id: RCV000229345 RCV000791433 RCV000755259 RCV002399723 RCV003907720
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Arg529His
CA321073
NM_001114753.3:c.1586G>A