Allele Registry

Canonical Allele Identifier: PA119708

Gene: EPHB2 HGNC NCBI

ClinVar RCV:

RCV000009059

RCV000894397

ClinVar Variation:

8533

HGVS (amino-acid)	Matching Registered Transcripts
NP_059145.2:p.Ala279Ser	CA119704 NM_017449.5:c.835G>T