Canonical Allele Identifier: PA2828579118
Gene: CSF1R HGNC NCBI

Linked Data

ClinVar Variation Id: 3005076
ClinVar RCV Id: RCV003868203

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362250.1:p.Ala151Val
CA3506991
NM_001375321.1:c.452C>T