Canonical Allele Identifier: PA2826581776
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 161229
ClinVar RCV Id: RCV000148482 RCV000243657 RCV000230696 RCV000756073 RCV001079415 RCV002408654
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Ser433Leu
CA211415
NM_001278138.2:c.1298C>T