Canonical Allele Identifier: PA645474140
Gene: CSF1R HGNC NCBI

Linked Data

ClinVar Variation Id: 376166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005202.2:p.Tyr571Asp
CA16602623
NM_005211.4:c.1711T>G