Canonical Allele Identifier: PA2825044052
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1475358
ClinVar RCV Id: RCV001976177
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Asn163Tyr
CA200314449
NM_000118.3:c.487A>T