Canonical Allele Identifier: PA2825043751
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 439647
ClinVar RCV Id: RCV000506963 RCV001377784
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Leu14Pro
CA374989588
NM_000118.3:c.41T>C