Canonical Allele Identifier: PA2828578679
Gene: CSF1R HGNC NCBI

Linked Data

ClinVar Variation Id: 1415854

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362249.1:p.Asn308Lys
CA3506989
NM_001375320.1:c.924C>G
CA361725183
NM_001375320.1:c.924C>A