Canonical Allele Identifier: PA111048
Gene: EDN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 16647
ClinVar RCV Id: RCV000214032 RCV000907433 RCV000990324 RCV000018127
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996917.1:p.Ala224Thr
CA126749
NM_207034.3:c.670G>A