Canonical Allele Identifier: PA916009952
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 407121
ClinVar RCV Id: RCV000460714 RCV001753879 RCV002365627
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Val56Glu
CA16612408
NM_001278138.2:c.167T>A