Canonical Allele Identifier: PA2826938758
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_001296122.1:p.Gly786Arg
CA678950
NM_001309193.2:c.2356G>A
CA338953881
NM_001309193.2:c.2356G>C