Canonical Allele Identifier: PA2825584958
Gene: EDNRB HGNC NCBI

Linked Data

ClinVar Variation Id: 870486
ClinVar RCV Id: RCV001090044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116131.1:p.Leu277Arg
CA501212
NM_001122659.3:c.830_831delinsGG
CA388452156
NM_001122659.3:c.830T>G