Allele Registry

Canonical Allele Identifier: PA112556

Gene: CTRC HGNC NCBI

ClinVar RCV:

RCV000119044

ClinVar Variation:

132149

HGVS (amino-acid)	Matching Registered Transcripts
NP_009203.2:p.Ala73Thr	CA345647 NM_007272.3:c.217G>A