Canonical Allele Identifier: PA2827263136
Gene: EPHA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 293416
ClinVar RCV Id: RCV000279994
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316019.1:p.Gly608Ser
CA624984
NM_001329090.2:c.1822G>A