Canonical Allele Identifier: PA2827936266
Gene: EDNRA HGNC NCBI

Linked Data

ClinVar Variation Id: 520836
ClinVar RCV Id: RCV000624539
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341726.1:p.Ser168Leu
CA358421770
NM_001354797.2:c.503C>T