Allele Registry

Canonical Allele Identifier: PA119712

Gene: EPHB2 HGNC NCBI

ClinVar RCV:

RCV000009060

RCV000974432

RCV003934813

ClinVar Variation:

8534

HGVS (amino-acid)	Matching Registered Transcripts
NP_059145.2:p.Asp678Asn	CA119709 NM_017449.5:c.2032G>A