Canonical Allele Identifier: PA2825044445
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1069311

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Met269Lys
CA374983058
NM_000118.3:c.806T>A