Allele Registry

Canonical Allele Identifier: PA645389038

Gene: EPHA2 HGNC NCBI

ClinVar RCV:

RCV000340843

ClinVar Variation:

293437

HGVS (amino-acid)	Matching Registered Transcripts
NP_004422.2:p.Pro350Thr	CA625332 NM_004431.5:c.1048C>A