Canonical Allele Identifier: PA2828579170
Gene: CSF1R HGNC NCBI

Linked Data

ClinVar Variation Id: 2713774
ClinVar RCV Id: RCV003550565

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362250.1:p.Arg251Gly
CA361721823
NM_001375321.1:c.751C>G