Canonical Allele Identifier: PA2825044472
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 528083
ClinVar RCV Id: RCV000633165 RCV001165467 RCV002292573 RCV002413813
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Glu284Lys
CA5252951
NM_000118.3:c.850G>A