Canonical Allele Identifier: PA2827510788
Gene: CSF1R HGNC NCBI

Linked Data

ClinVar Variation Id: 2133223
ClinVar RCV Id: RCV003056234
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336665.1:p.Thr314Ile
CA361725011
NM_001349736.2:c.941C>T