Canonical Allele Identifier: PA2825274379
Gene: EDA HGNC NCBI
ClinVar RCV:
RCV001551029
ClinVar Variation:
1190348
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005612.2:p.Pro203Thr
CA413448337
NM_001005612.3:c.607C>A