Canonical Allele Identifier: PA2825274006
Gene: EDA HGNC NCBI
ClinVar RCV:
RCV000413515
ClinVar Variation:
372608
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005609.1:p.Gly257Arg
CA16043329
NM_001005609.2:c.769G>C
CA413448690
NM_001005609.2:c.769G>A