Canonical Allele Identifier: PA645498577
Gene: EPHB4 HGNC NCBI

Linked Data

ClinVar Variation Id: 222000
ClinVar RCV Id: RCV000408650
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004435.3:p.Pro327Leu
CA10602395
NM_004444.5:c.980C>T