Canonical Allele Identifier: PA2573233698
Gene: FADD HGNC NCBI

Linked Data

ClinVar Variation Id: 1494177
ClinVar RCV Id: RCV002012815
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003815.1:p.Ile104Val
CA381665917
NM_003824.4:c.310A>G