ClinGen Allele Registry
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Canonical Allele Identifier:
PA2828759195
Gene: EPHX1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000018075
RCV000991132
RCV001610293
ClinVar Variation:
16604
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001365357.1:p.Tyr104His
CA126706
NM_001378428.1:c.310T>C