Canonical Allele Identifier: PA2826790734
Gene: FAT4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1712536
ClinVar RCV Id: RCV002300708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278214.1:p.Thr780Ser
CA358120107
NM_001291285.3:c.2338A>T
CA358120109
NM_001291285.3:c.2339C>G