ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826397285
Gene: EPHX2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
3059509
ClinVar RCV Id:
RCV003974480
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001243413.1:p.Lys2Arg
CA4689907
NM_001256484.2:c.5A>G