Canonical Allele Identifier: PA133742
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 44185
ClinVar RCV Id: RCV000037161 RCV000542700 RCV000624502 RCV001577971 RCV003485530 RCV004545739
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Val365Ala
CA133741
NM_001399.5:c.1094T>C