Canonical Allele Identifier: PA916057853
Gene: EDARADD HGNC NCBI

Linked Data

ClinVar Variation Id: 262601

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542776.1:p.Ser93Phe
CA1470064
NM_080738.4:c.278C>T