Canonical Allele Identifier: PA1139689673
Gene: EDNRB HGNC NCBI

Linked Data

ClinVar Variation Id: 870486
ClinVar RCV Id: RCV001090044
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001188326.1:p.Leu367Arg
CA501212
NM_001201397.1:c.1100_1101delinsGG
CA388452156
NM_001201397.1:c.1100T>G