Allele Registry

Canonical Allele Identifier: PA112597

Gene: CTRC HGNC NCBI

ClinVar RCV:

RCV000483666

RCV001856839

ClinVar Variation:

420177

HGVS (amino-acid)	Matching Registered Transcripts
NP_009203.2:p.Gly217Arg	CA16616982 NM_007272.3:c.649G>C