Canonical Allele Identifier: PA645453190
Gene: EDNRB HGNC NCBI

Linked Data

ClinVar Variation Id: 226623

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000106.1:p.Leu17Phe
CA7012405
NM_000115.5:c.49C>T