Allele Registry

Canonical Allele Identifier: PA2827263137

Gene: EPHA2 HGNC NCBI

ClinVar RCV:

RCV000171149

ClinVar Variation:

190978

HGVS (amino-acid)	Matching Registered Transcripts
NP_001316019.1:p.Gln615His	CA235737 NM_001329090.2:c.1845G>T CA338624085 NM_001329090.2:c.1845G>C