Canonical Allele Identifier: PA2827510931
Gene: CSF1R HGNC NCBI

Linked Data

ClinVar Variation Id: 162127

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336665.1:p.Leu582Pro
CA346100
NM_001349736.2:c.1745T>C