Canonical Allele Identifier: PA102373
Gene: EDNRB HGNC NCBI

Linked Data

ClinVar Variation Id: 16634
ClinVar RCV Id: RCV000018114
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000106.1:p.Ala183Gly
CA126744
NM_000115.5:c.548C>G