Canonical Allele Identifier: PA658676760
Gene: EDA HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Val324Met
CA413449530
NM_001399.5:c.970G>A