Canonical Allele Identifier: PA2825044708
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 2957089
ClinVar RCV Id: RCV003818776
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Ala408Val
CA5252843
NM_000118.3:c.1223C>T