Canonical Allele Identifier: PA2825274628
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 11032
ClinVar RCV Id: RCV000011779 RCV000218834 RCV000432524 RCV003894799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005613.1:p.Arg69Leu
CA255650
NM_001005613.4:c.206G>T