Canonical Allele Identifier: PA2825044588
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1024698
ClinVar RCV Id: RCV001324912
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Gln342His
CA374981698
NM_000118.3:c.1026G>T
CA374981700
NM_000118.3:c.1026G>C