Canonical Allele Identifier: PA2827510777
Gene: CSF1R HGNC NCBI

Linked Data

ClinVar Variation Id: 3005076
ClinVar RCV Id: RCV003868203

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336665.1:p.Ala299Val
CA3506991
NM_001349736.2:c.896C>T