Canonical Allele Identifier: PA2825850869
Gene: EYS HGNC NCBI

Linked Data

ClinVar Variation Id: 1392579
ClinVar RCV Id: RCV001911286
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136272.1:p.Thr2559Ala
CA364384929
NM_001142800.2:c.7675A>G