Canonical Allele Identifier: PA2827510923
Gene: CSF1R HGNC NCBI

Linked Data

ClinVar Variation Id: 376166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336665.1:p.Tyr571Asp
CA16602623
NM_001349736.2:c.1711T>G