Canonical Allele Identifier: PA2825044728
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 528061
ClinVar RCV Id: RCV002233945
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Met420Thr
CA5252838
NM_000118.3:c.1259T>C