Canonical Allele Identifier: PA658803114
Gene: ENG HGNC NCBI
ClinVar RCV:
RCV000633140
ClinVar Variation:
528060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Ser615Trp
CA5252623
NM_001114753.3:c.1844C>G