Canonical Allele Identifier: PA126753
Gene: EDN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 16650
ClinVar RCV Id: RCV000018130

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996917.1:p.His112Arg
CA126752
NM_207034.3:c.335A>G