Canonical Allele Identifier: PA2825044562
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 407115
ClinVar RCV Id: RCV000462769 RCV000791420 RCV001531114 RCV002379438
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Gly331Ser
CA16612528
NM_000118.3:c.991G>A