Canonical Allele Identifier: PA2825044469
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 574807
ClinVar RCV Id: RCV002233320
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Lys280Arg
CA5252953
NM_000118.3:c.839A>G