Canonical Allele Identifier: PA645454400
Gene: EDNRB HGNC NCBI

Linked Data

ClinVar Variation Id: 16638
ClinVar RCV Id: RCV000018118 RCV000222856 RCV000626404 RCV000659497 RCV000954472 RCV001258252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001188326.1:p.Ser395Asn
CA257563
NM_001201397.1:c.1184G>A