Canonical Allele Identifier: PA645384980
Gene: EDARADD HGNC NCBI

Linked Data

ClinVar Variation Id: 262601

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665860.2:p.Ser103Phe
CA1470064
NM_145861.4:c.308C>T