Canonical Allele Identifier: PA645397500
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_004433.2:p.Gly787Arg
CA678950
NM_004442.7:c.2359G>A
CA338953881
NM_004442.7:c.2359G>C