Canonical Allele Identifier: PA2826712645
Gene: CSF1R HGNC NCBI

Linked Data

ClinVar Variation Id: 3005076
ClinVar RCV Id: RCV003868203

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275634.1:p.Ala299Val
CA3506991
NM_001288705.3:c.896C>T