Canonical Allele Identifier: PA2573094018
Gene: FAM20C HGNC NCBI

Linked Data

ClinVar Variation Id: 30875
ClinVar RCV Id: RCV000023860 RCV002468976
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064608.2:p.Asp451Asn
CA366525682
NM_020223.4:c.1351G>A