Canonical Allele Identifier: PA2825044675
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1734239
ClinVar RCV Id: RCV002349040
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Ile384Ser
CA374978829
NM_000118.3:c.1151T>G