Canonical Allele Identifier: PA2742033032
Gene: FAM83H HGNC NCBI

Linked Data

ClinVar Variation Id: 2622030
ClinVar RCV Id: RCV003386644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_940890.4:p.Arg293His
CA4917564
NM_198488.5:c.878G>A