Canonical Allele Identifier: PA2825044391
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 645651
ClinVar RCV Id: RCV000799784
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Asp248Asn
CA5252997
NM_000118.3:c.742G>A