Canonical Allele Identifier: PA1139687232
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 937612
ClinVar RCV Id: RCV001206664
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Met87Arg
CA374983056
NM_001278138.2:c.260T>G