Allele Registry

Canonical Allele Identifier: PA2826371725

Gene: CTHRC1 HGNC NCBI

ClinVar Variation Id: 2204836

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243028.1:p.Ser128Arg	CA4835251 NM_001256099.2:c.382A>C CA371634879 NM_001256099.2:c.384T>A CA371634880 NM_001256099.2:c.384T>G