Canonical Allele Identifier: PA101244
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 237027
ClinVar RCV Id: RCV000231233 RCV000427340 RCV002223199 RCV002494618 RCV002327101 RCV003422129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Trp149Cys
CA10582615
NM_001114753.3:c.447G>C
CA374984252
NM_001114753.3:c.447G>T