Canonical Allele Identifier: PA916009936
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 161233
ClinVar RCV Id: RCV000148487 RCV000457880 RCV000859971 RCV003298151 RCV003407567 RCV000488867
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Gly32Ser
CA211422
NM_001278138.2:c.94G>A