Canonical Allele Identifier: PA100721
Gene: EDN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 120213
ClinVar RCV Id: RCV000106313

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001946.3:p.Pro77His
CA150780
NM_001955.5:c.230C>A