Canonical Allele Identifier: PA645495527
Gene: FAM20C HGNC NCBI

Linked Data

ClinVar Variation Id: 290748
ClinVar RCV Id: RCV000270050 RCV003243048 RCV002518145 RCV003930189
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064608.2:p.Pro67His
CA4108891
NM_020223.4:c.200C>A