Canonical Allele Identifier: PA102430
Gene: EDNRB HGNC NCBI

Linked Data

ClinVar Variation Id: 16633

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000106.1:p.Trp276Cys
CA126743
NM_000115.5:c.828G>T
CA388452161
NM_000115.5:c.828G>C