Canonical Allele Identifier: PA2826581531
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1015736
ClinVar RCV Id: RCV001314641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Arg217Ser
CA374978541
NM_001278138.2:c.651G>T
CA374978543
NM_001278138.2:c.651G>C