Canonical Allele Identifier: PA2826712705
Gene: CSF1R HGNC NCBI

Linked Data

ClinVar Variation Id: 2153358
ClinVar RCV Id: RCV003085623

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275634.1:p.Arg399Gln
CA3506932
NM_001288705.3:c.1196G>A