Canonical Allele Identifier: PA2825044702
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1415156
ClinVar RCV Id: RCV001945484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Arg406Cys
CA5252846
NM_000118.3:c.1216C>T