Canonical Allele Identifier: PA2826581525
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1024161
ClinVar RCV Id: RCV001324312
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Asp209His
CA374978704
NM_001278138.2:c.625G>C