Canonical Allele Identifier: PA645400216
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 407131
ClinVar RCV Id: RCV000469330 RCV000508379 RCV002230780 RCV002418369
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Met1Val