Canonical Allele Identifier: PA916009958
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 582982
ClinVar RCV Id: RCV000707190
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Gly63Arg
CA5252998
NM_001278138.2:c.187G>A
CA374983390
NM_001278138.2:c.187G>C