Canonical Allele Identifier: PA2826581502
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1701581
ClinVar RCV Id: RCV002276212 RCV002434618 RCV003096217 RCV003138147
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Lys192Ser
CA913186018
NM_001278138.2:c.575_576delinsGC