Canonical Allele Identifier: PA2825274198
Gene: EDA HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005610.2:p.Leu55Gln
CA261482
NM_001005610.4:c.164T>A