Allele Registry

Canonical Allele Identifier: PA645464755

Gene: CTRC HGNC NCBI

ClinVar RCV:

RCV000305597

ClinVar Variation:

292907

HGVS (amino-acid)	Matching Registered Transcripts
NP_009203.2:p.Ala28Thr	CA613211 NM_007272.3:c.82G>A