Canonical Allele Identifier: PA2825044691
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1015736
ClinVar RCV Id: RCV001314641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Arg399Ser
CA374978541
NM_000118.3:c.1197G>T
CA374978543
NM_000118.3:c.1197G>C