Canonical Allele Identifier: PA202696
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 161232
ClinVar RCV Id: RCV000148486 RCV000178045 RCV000346221 RCV000857942 RCV001258238 RCV001588996 RCV002371988
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Pro131Leu
CA202695
NM_000118.3:c.392C>T