Canonical Allele Identifier: PA2828579117
Gene: CSF1R HGNC NCBI

Linked Data

ClinVar Variation Id: 904114

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362250.1:p.Ala151Thr
CA3506992
NM_001375321.1:c.451G>A