Canonical Allele Identifier: PA2825584956
Gene: EDNRB HGNC NCBI

Linked Data

ClinVar Variation Id: 16633
ClinVar RCV Id: RCV000018113 RCV000018112 RCV003236768
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116131.1:p.Trp276Cys
CA126743
NM_001122659.3:c.828G>T
CA388452161
NM_001122659.3:c.828G>C