Canonical Allele Identifier: PA2828619512
Gene: FOCAD HGNC NCBI

Linked Data

ClinVar Variation Id: 402871
ClinVar RCV Id: RCV000455620 RCV001653792 RCV003972705
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362499.1:p.Leu131Ser
CA5006387
NM_001375570.1:c.392T>C