Canonical Allele Identifier: PA2827510779
Gene: CSF1R HGNC NCBI

Linked Data

ClinVar Variation Id: 376273

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336665.1:p.Leu301Ser
CA16602721
NM_001349736.2:c.902T>C