Canonical Allele Identifier: PA2825044652
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1794612
ClinVar RCV Id: RCV002428851
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Leu370Pro
CA374980705
NM_000118.3:c.1109T>C