Canonical Allele Identifier: PA2829866296
Gene: EPHB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 376739
ClinVar RCV Id: RCV000434509
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_059145.2:p.Gly786Arg
CA678950
NM_017449.5:c.2356G>A
CA338953881
NM_017449.5:c.2356G>C