Canonical Allele Identifier: PA2825044686
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_000109.1:p.Asp391His
CA374978704
NM_000118.3:c.1171G>C