Canonical Allele Identifier: PA2825273935
Gene: EDA HGNC NCBI

Linked Data

ClinVar Variation Id: 1675183
ClinVar RCV Id: RCV002210930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005609.1:p.Ser160Arg
CA413447988
NM_001005609.2:c.478A>C
CA413447994
NM_001005609.2:c.480C>A
CA413447995
NM_001005609.2:c.480C>G