Canonical Allele Identifier: PA257562
Gene: EDNRB HGNC NCBI

Linked Data

ClinVar Variation Id: 16637
ClinVar RCV Id: RCV000018117 RCV000216329 RCV000224294
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000106.1:p.Gly57Ser
CA257561
NM_000115.5:c.169G>A