Canonical Allele Identifier: PA2825044507
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 528052

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Arg304Gln
CA5252939
NM_000118.3:c.911G>A