Canonical Allele Identifier: PA2825044992
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1013753
ClinVar RCV Id: RCV001312394
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Cys582Gly
CA374972338
NM_000118.3:c.1744T>G