Canonical Allele Identifier: PA1139731082
Gene: CSF1R HGNC NCBI

Linked Data

ClinVar Variation Id: 904114

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005202.2:p.Ala299Thr
CA3506992
NM_005211.4:c.895G>A