Canonical Allele Identifier: PA645389088
Gene: EPHA2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004422.2:p.Gly662Ser
CA624984
NM_004431.5:c.1984G>A