Canonical Allele Identifier: PA2825044670
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_000109.1:p.Cys382Tyr
CA374978902
NM_000118.3:c.1145G>A