Canonical Allele Identifier: PA2828579271
Gene: CSF1R HGNC NCBI

Linked Data

ClinVar Variation Id: 162127

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362250.1:p.Leu434Pro
CA346100
NM_001375321.1:c.1301T>C