Allele Registry

Canonical Allele Identifier: PA915988868

Gene: CALCR HGNC NCBI

ClinVar RCV:

RCV000019203

RCV001642229

RCV003974841

ClinVar Variation:

17636

HGVS (amino-acid)	Matching Registered Transcripts
NP_001158209.2:p.Leu463Pro	CA127309 NM_001164737.3:c.1388T>C