Canonical Allele Identifier: PA278846
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_004422.2:p.Phe660Val
CA278845
NM_004431.5:c.1978T>G