Canonical Allele Identifier: PA2826002837
Gene: CALCR HGNC NCBI

Linked Data

ClinVar Variation Id: 2527780
ClinVar RCV Id: RCV004301054
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158210.1:p.Ser422Cys
CA162017960
NM_001164738.2:c.1265C>G