Canonical Allele Identifier: PA2826581512
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 430375
ClinVar RCV Id: RCV000494433 RCV002455955 RCV002524049
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Cys200Tyr
CA374978902
NM_001278138.2:c.599G>A