Canonical Allele Identifier: PA2825044712
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 458332
ClinVar RCV Id: RCV000547986 RCV002367790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Cys412Tyr
CA374978391
NM_000118.3:c.1235G>A