Canonical Allele Identifier: PA250058
Gene: FAM20C HGNC NCBI

Linked Data

ClinVar Variation Id: 30876
ClinVar RCV Id: RCV000023861
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064608.2:p.Ile246Asn
CA250057
NM_020223.4:c.737T>A