Canonical Allele Identifier: PA645389079
Gene: EPHA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 293423
ClinVar RCV Id: RCV000403532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004422.2:p.Arg615Trp
CA10608023
NM_004431.5:c.1843C>T