Canonical Allele Identifier: PA2828579129
Gene: CSF1R HGNC NCBI

Linked Data

ClinVar Variation Id: 2133223
ClinVar RCV Id: RCV003056234

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362250.1:p.Thr166Ile
CA361725011
NM_001375321.1:c.497C>T