Canonical Allele Identifier: PA126755
Gene: EDN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 16651
ClinVar RCV Id: RCV000018131
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996917.1:p.Arg93Gly
CA126754
NM_207034.3:c.277C>G