Canonical Allele Identifier: PA1139708850
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 849399
ClinVar RCV Id: RCV001053348
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Pro203Leu
CA413448340
NM_001399.5:c.608C>T