Allele Registry

Canonical Allele Identifier: PA119713

Gene: EPHB2 HGNC NCBI

ClinVar RCV:

RCV000009060

RCV000974432

RCV003934813

ClinVar Variation:

8534

HGVS (amino-acid)	Matching Registered Transcripts
NP_004433.2:p.Asp679Asn	CA119709 NM_004442.7:c.2035G>A