Canonical Allele Identifier: PA2825045026
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 528060
ClinVar RCV Id: RCV000633140
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Ser615Trp
CA5252623
NM_000118.3:c.1844C>G