Canonical Allele Identifier: PA1139687153
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 938575
ClinVar RCV Id: RCV001207824
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Arg50Gln
CA5253011
NM_001278138.2:c.149G>A