Canonical Allele Identifier: PA2580146261
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1782359
ClinVar RCV Id: RCV002408314 RCV003418519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Ser635Leu
CA5252585
NM_001114753.3:c.1904C>T