Canonical Allele Identifier: PA2825274535
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 228255
ClinVar RCV Id: RCV000809933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005612.2:p.Ala351Val
CA10577181
NM_001005612.3:c.1052C>T