Canonical Allele Identifier: PA2825044986
Gene: ENG HGNC NCBI
ClinVar RCV:
RCV000706057
ClinVar Variation:
582079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Ser576Gly
CA374973482
NM_000118.3:c.1726A>G