Canonical Allele Identifier: PA2580150971
Gene: CALCR HGNC NCBI

Linked Data

ClinVar Variation Id: 2215006
ClinVar RCV Id: RCV004075835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158209.2:p.Arg432His
CA4345297
NM_001164737.3:c.1295G>A