Canonical Allele Identifier: PA2826581648
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1404798
ClinVar RCV Id: RCV001903408

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Phe304Leu
CA374975997
NM_001278138.2:c.912C>G
CA374975998
NM_001278138.2:c.912C>A
CA374976014
NM_001278138.2:c.910T>C