Canonical Allele Identifier: PA200753
Gene: FAM20C HGNC NCBI

Linked Data

ClinVar Variation Id: 193729
ClinVar RCV Id: RCV000173883 RCV000224271 RCV002500462
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064608.2:p.Val561Met
CA200752
NM_020223.4:c.1681G>A