Canonical Allele Identifier: PA2825274066
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 1044137
ClinVar RCV Id: RCV001348345
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005609.1:p.Ser305Asn
CA413449039
NM_001005609.2:c.914G>A