Canonical Allele Identifier: PA346101
Gene: CSF1R HGNC NCBI

Linked Data

ClinVar Variation Id: 162127

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005202.2:p.Leu582Pro
CA346100
NM_005211.4:c.1745T>C