Canonical Allele Identifier: PA105100
Gene: FAM20C HGNC NCBI

Linked Data

ClinVar Variation Id: 1024
ClinVar RCV Id: RCV000001079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064608.2:p.Leu388Arg
CA250012
NM_020223.4:c.1163T>G