Canonical Allele Identifier: PA100301
Gene: EDARADD HGNC NCBI

Linked Data

ClinVar Variation Id: 4189

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665860.2:p.Leu122Arg
CA019395
NM_145861.4:c.365T>G