Canonical Allele Identifier: PA2826581769
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 995600
ClinVar RCV Id: RCV001289606 RCV002411932 RCV003594127
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Gly421Arg
CA374971981
NM_001278138.2:c.1261G>C
CA374971982
NM_001278138.2:c.1261G>A