Allele Registry

Canonical Allele Identifier: PA2827263059

Gene: EPHA2 HGNC NCBI

ClinVar RCV:

RCV000340843

ClinVar Variation:

293437

HGVS (amino-acid)	Matching Registered Transcripts
NP_001316019.1:p.Pro296Thr	CA625332 NM_001329090.2:c.886C>A