Canonical Allele Identifier: PA2827263134
Gene: EPHA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 217349
ClinVar RCV Id: RCV000203400
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316019.1:p.Phe606Val
CA278845
NM_001329090.2:c.1816T>G