Canonical Allele Identifier: PA2826938662
Gene: EPHB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 786983
ClinVar RCV Id: RCV000969133
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001296121.1:p.Val592Ala
CA678850
NM_001309192.2:c.1775T>C