Canonical Allele Identifier: PA2825044843
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 458338
ClinVar RCV Id: RCV000539445 RCV002395314
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Leu490Ser
CA5252752
NM_000118.3:c.1469T>C