Allele Registry

Canonical Allele Identifier: PA126757

Gene: EDN1 HGNC NCBI

ClinVar RCV:

RCV000018132

RCV000835753

RCV001659700

ClinVar Variation:

16652

HGVS (amino-acid)	Matching Registered Transcripts
NP_001946.3:p.Lys198Asn	CA126756 NM_001955.5:c.594G>T CA362857349 NM_001955.5:c.594G>C