Allele Registry

Canonical Allele Identifier: PA127311

Gene: CALCR HGNC NCBI

ClinVar RCV:

RCV000019203

RCV001642229

RCV003974841

ClinVar Variation:

17636

HGVS (amino-acid)	Matching Registered Transcripts
NP_001733.1:p.Leu447Pro	CA127309 NM_001742.4:c.1340T>C