Canonical Allele Identifier: PA2827510829
Gene: CSF1R HGNC NCBI

Linked Data

ClinVar Variation Id: 2713774
ClinVar RCV Id: RCV003550565
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336665.1:p.Arg399Gly
CA361721823
NM_001349736.2:c.1195C>G