Canonical Allele Identifier: PA111057
Gene: EDN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 16644
ClinVar RCV Id: RCV000018124

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996917.1:p.Cys159Phe
CA126747
NM_207034.3:c.476G>T