Canonical Allele Identifier: PA2828579142
Gene: CSF1R HGNC NCBI

Linked Data

ClinVar Variation Id: 1936321
ClinVar RCV Id: RCV002636357

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362250.1:p.Asp196Phe
CA2580073858
NM_001375321.1:c.586_587delinsTT