Canonical Allele Identifier: PA645484060
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 379815
ClinVar RCV Id: RCV000439320 RCV000526582
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001390.1:p.Pro206Leu
CA16608975
NM_001399.5:c.617C>T