ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826938665
Gene: EPHB2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000009060
RCV000974432
RCV003934813
ClinVar Variation:
8534
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001296121.1:p.Asp620Asn
CA119709
NM_001309192.2:c.1858G>A