Canonical Allele Identifier: PA116680
Gene: EDARADD HGNC NCBI

Linked Data

ClinVar Variation Id: 4189

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542776.1:p.Leu112Arg
CA019395
NM_080738.4:c.335T>G